Canonical Allele Identifier: CA1877041930
Gene:

Linked Data

dbSNP Id: rs1771889

Genomic Alleles

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

Transcript Alleles

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