Canonical Allele Identifier: CA1674890160
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817521T= , CM000668.2:g.155817521T= GRCh38
NC_000006.11:g.156138655T= , CM000668.1:g.156138655T= GRCh37
NC_000006.10:g.156180347T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24102T=
XR_943146.1:n.552-2851A=
XR_001744423.1:n.606-2851A=
XR_001744424.1:n.79+24102T=