Canonical Allele Identifier: CA11080660
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.121054648A>G , CM000664.2:g.121054648A>G GRCh38
NC_000002.11:g.121812224A>G , CM000664.1:g.121812224A>G GRCh37
NC_000002.10:g.121528694A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923264.1:n.1027-1739A>G
XR_923265.1:n.227-1739A>G
XR_923266.1:n.1027-1806A>G
XR_923267.1:n.199-1739A>G
XR_923268.1:n.1035A>G