Canonical Allele Identifier: CA1609069988
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525279C= , CM000668.2:g.8525279C= GRCh38
NC_000006.11:g.8525512C= , CM000668.1:g.8525512C= GRCh37
NC_000006.10:g.8470511C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038979.1:n.626-33306C=
NR_038980.1:n.649-33306C=