Canonical Allele Identifier: CA13633930
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115453598C>T , CM000674.2:g.115453598C>T GRCh38
NC_000012.11:g.115891403C>T , CM000674.1:g.115891403C>T GRCh37
NC_000012.10:g.114375786C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945388.1:n.461-46267G>A
XR_945389.1:n.461-46267G>A
XR_945388.2:n.465-46267G>A
XR_945389.2:n.465-46267G>A