Canonical Allele Identifier: CA1595159066
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580733A= , CM000667.2:g.159580733A= GRCh38
NC_000005.9:g.159007741A= , CM000667.1:g.159007741A= GRCh37
NC_000005.8:g.158940319A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+298A=
XR_941140.1:n.2075+298A=
XR_941141.1:n.570+298A=
XR_941139.2:n.2229+298A=