Canonical Allele Identifier: CA2336337469
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41167943G>A , CM000681.2:g.41167943G>A GRCh38
NC_000019.9:g.41673848G>A , CM000681.1:g.41673848G>A GRCh37
NC_000019.8:g.46365688G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011527591.1:c.184+8016C>T XP_011525893.1:n.184+8016C>T