Canonical Allele Identifier: CA1674890295
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817692A= , CM000668.2:g.155817692A= GRCh38
NC_000006.11:g.156138826A= , CM000668.1:g.156138826A= GRCh37
NC_000006.10:g.156180518A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24273A=
XR_943146.1:n.552-3022T=
XR_001744423.1:n.606-3022T=
XR_001744424.1:n.79+24273A=