Canonical Allele Identifier: CA1605281523
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.475489C= , CM000668.2:g.475489C= GRCh38
NC_000006.11:g.475489C= , CM000668.1:g.475489C= GRCh37
NC_000006.10:g.420489C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2715-9204C=
XR_926365.1:n.2549-9204C=
XR_001743914.1:n.763C=