Canonical Allele Identifier: CA1674890282
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817683A= , CM000668.2:g.155817683A= GRCh38
NC_000006.11:g.156138817A= , CM000668.1:g.156138817A= GRCh37
NC_000006.10:g.156180509A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+24264A=
XR_943146.1:n.552-3013T=
XR_001744423.1:n.606-3013T=
XR_001744424.1:n.79+24264A=