Canonical Allele Identifier: CA20004397
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.28873487C>T , CM000663.2:g.28873487C>T GRCh38
NC_000001.10:g.29199999C>T , CM000663.1:g.29199999C>T GRCh37
NC_000001.9:g.29072586C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947126.1:n.307-1090G>A
XR_001737953.2:n.343-999G>A