Canonical Allele Identifier: CA2122202191
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20793472C= , CM000676.2:g.20793472C= GRCh38
NC_000014.8:g.21261631C= , CM000676.1:g.21261631C= GRCh37
NC_000014.7:g.20331471C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943584.1:n.585+686C=
XR_943585.1:n.585+686C=
XR_001750620.1:n.3271+686C=
XR_001750621.1:n.3271+686C=
XR_001750622.1:n.637+6432G=
XR_001750623.1:n.637+6432G=
XR_001750624.1:n.637+6432G=