Canonical Allele Identifier: CA1605276841
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465886C= , CM000668.2:g.465886C= GRCh38
NC_000006.11:g.465886C= , CM000668.1:g.465886C= GRCh37
NC_000006.10:g.410886C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12161C=
XR_926365.1:n.2548+12161C=
XR_001743914.1:n.482-9322C=