Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 1:45013933 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910388

Most severe consequence
Clinical significance

Synonyms

LSDB 4801

This variation has 18 HGVS names - click the plus to show

1:g.45013933G>A
ENST00000462688.2:n.626G>A
ENST00000491773.2:n.653G>A
ENST00000428106.1:c.454+142G>A
ENST00000494399.2:n.639G>A
ENST00000469548.2:n.695G>A
ENST00000478467.2:n.502G>A
ENST00000486699.2:n.619G>A
ENST00000434478.2:c.436G>A
ENSP00000404489.1:p.Glu146Lys
ENST00000490385.2:n.573G>A
ENST00000460334.2:n.526G>A
ENST00000496439.1:n.595G>A
ENST00000491300.2:n.618G>A
ENST00000473012.1:n.546G>A
ENST00000246337.5:c.499G>A
ENSP00000246337.4:p.Glu167Lys
ENST00000460906.2:n.633G>A

Variation displays