Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 11:124872919 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041428

Most severe consequence
Clinical significance

Synonyms

LSDB 15852

This variation has 5 HGVS names - click the plus to show

11:g.124872919G>T
ENST00000538940.2:c.1300G>T
ENSP00000441797.1:p.Gly434Ter
ENST00000397801.2:c.1366G>T
ENSP00000380903.1:p.Gly456Ter

Variation displays