Canonical Allele Identifier: CA1609069983
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525268C= , CM000668.2:g.8525268C= GRCh38
NC_000006.11:g.8525501C= , CM000668.1:g.8525501C= GRCh37
NC_000006.10:g.8470500C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038979.1:n.626-33317C=
NR_038980.1:n.649-33317C=