Canonical Allele Identifier: CA1674885875
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812637T= , CM000668.2:g.155812637T= GRCh38
NC_000006.11:g.156133771T= , CM000668.1:g.156133771T= GRCh37
NC_000006.10:g.156175463T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19218T=
XR_943146.1:n.645-598A=
XR_001744423.1:n.699-598A=
XR_001744424.1:n.79+19218T=