Canonical Allele Identifier: CA756214983
Gene:

Linked Data

dbSNP Id: rs1183427067

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884058A>G , CM000664.2:g.122884058A>G GRCh38
NC_000002.11:g.123641634A>G , CM000664.1:g.123641634A>G GRCh37
NC_000002.10:g.123358104A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-884A>G
XR_001739692.1:n.1451-884A>G
XR_923292.2:n.1358-884A>G