Canonical Allele Identifier: CA12999800
Gene:

Linked Data

dbSNP Id: rs1771889

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.121370602A>G , CM000671.2:g.121370602A>G GRCh38
NC_000009.11:g.124132880A>G , CM000671.1:g.124132880A>G GRCh37
NC_000009.10:g.123172701A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930319.1:n.156A>G
XR_930320.1:n.159A>G
XR_930321.1:n.157A>G
XR_930322.1:n.157A>G
XR_001746556.2:n.158A>G
XR_001746557.2:n.157A>G
XR_001746558.2:n.158A>G
XR_001746559.2:n.158A>G
XR_930319.3:n.158A>G