Canonical Allele Identifier: CA1199280380
Gene:

Linked Data

dbSNP Id: rs1650971798

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147089033A>G , CM000663.2:g.147089033A>G GRCh38
NC_000001.10:g.146560580A>G , CM000663.1:g.146560580A>G GRCh37
NC_000001.9:g.145027204A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000444082.1:n.1845+20829T>C