Canonical Allele Identifier: CA2255112061
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237371A= , CM000679.2:g.30237371A= GRCh38
NC_000017.10:g.28564389A= , CM000679.1:g.28564389A= GRCh37
NC_000017.9:g.25588515A= NCBI36
NG_011747.2:g.3566T=

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.166-271A=
XR_001752824.1:n.281-271A=