Canonical Allele Identifier: CA1643745232
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.85982279C= , CM000668.2:g.85982279C= GRCh38
NC_000006.11:g.86691997C= , CM000668.1:g.86691997C= GRCh37
NC_000006.10:g.86748716C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_241869.3:n.615-11101C=
XR_942747.1:n.41-1090C=
XR_942748.1:n.27-1090C=
XR_001744239.1:n.1570-11101C=
XR_001744243.1:n.1433-11101C=
XR_002956361.1:n.1992-11101C=