Canonical Allele Identifier: CA1674890316
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817723A= , CM000668.2:g.155817723A= GRCh38
NC_000006.11:g.156138857A= , CM000668.1:g.156138857A= GRCh37
NC_000006.10:g.156180549A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+24304A=
XR_943146.1:n.552-3053T=
XR_001744423.1:n.606-3053T=
XR_001744424.1:n.79+24304A=