Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 19:45768373 (forward strand) | View in location tab

Co-located

with COSMIC COSM126184 (C/A) ; HGMD-PUBLIC CM071085

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_175875.3:c.472G>A, 2010_April_001_099_SIX5_600963_0001, 9734

This variation has 9 HGVS names - click the plus to show

19:g.45768373C>T
ENST00000622857.1:c.15+457G>A
ENST00000590076.2:n.336+242C>T
ENST00000559756.1:n.1181-459C>T
ENST00000560160.1:c.255G>A
ENSP00000453239.2:p.Ala86Thr
ENST00000560168.1:c.131-261G>A
ENST00000317578.6:c.472G>A
ENSP00000316842.4:p.Ala158Thr

Variation displays