Canonical Allele Identifier: CA1609069947
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525164C= , CM000668.2:g.8525164C= GRCh38
NC_000006.11:g.8525397C= , CM000668.1:g.8525397C= GRCh37
NC_000006.10:g.8470396C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038979.1:n.626-33421C=
NR_038980.1:n.649-33421C=