Canonical Allele Identifier: CA1674885886
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812650G= , CM000668.2:g.155812650G= GRCh38
NC_000006.11:g.156133784G= , CM000668.1:g.156133784G= GRCh37
NC_000006.10:g.156175476G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19231G=
XR_943146.1:n.645-611C=
XR_001744423.1:n.699-611C=
XR_001744424.1:n.79+19231G=