Canonical Allele Identifier: CA1769514505
Gene:

Linked Data

dbSNP Id: rs1799794821

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734873T>A , CM000670.2:g.20734873T>A GRCh38
NC_000008.10:g.20592384T>A , CM000670.1:g.20592384T>A GRCh37
NC_000008.9:g.20636664T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949569.3:n.72-55573T>A