Canonical Allele Identifier: CA1674885984
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812733C= , CM000668.2:g.155812733C= GRCh38
NC_000006.11:g.156133867C= , CM000668.1:g.156133867C= GRCh37
NC_000006.10:g.156175559C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19314C=
XR_943146.1:n.645-694G=
XR_001744423.1:n.699-694G=
XR_001744424.1:n.79+19314C=