Canonical Allele Identifier: CA1674885597
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812368T= , CM000668.2:g.155812368T= GRCh38
NC_000006.11:g.156133502T= , CM000668.1:g.156133502T= GRCh37
NC_000006.10:g.156175194T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18949T=
XR_943146.1:n.645-329A=
XR_001744423.1:n.699-329A=
XR_001744424.1:n.79+18949T=