Original source

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

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

Chromosome 11:64746796 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001321

Most severe consequence
Clinical significance

Synonyms

LSDB 15736

This variation has 7 HGVS names - click the plus to show

11:g.64746796A>G
ENST00000483742.1:n.1745T>C
ENST00000377432.5:c.2128T>C
ENSP00000366650.3:p.Trp710Arg
ENST00000164139.3:c.2392T>C
ENSP00000164139.3:p.Trp798Arg
LRG_100:g.3661T>C

Variation displays