Canonical Allele Identifier: CA1674890161
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817523T= , CM000668.2:g.155817523T= GRCh38
NC_000006.11:g.156138657T= , CM000668.1:g.156138657T= GRCh37
NC_000006.10:g.156180349T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24104T=
XR_943146.1:n.552-2853A=
XR_001744423.1:n.606-2853A=
XR_001744424.1:n.79+24104T=