Canonical Allele Identifier: CA11216571
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127135234C>T , CM000664.2:g.127135234C>T GRCh38
NC_000002.11:g.127892810C>T , CM000664.1:g.127892810C>T GRCh37
NC_000002.10:g.127609280C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923310.1:n.505-26C>T
XR_923311.1:n.557-26C>T
XR_923310.2:n.505-26C>T
XR_923311.3:n.662-26C>T