Canonical Allele Identifier: CA2122202281
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20793560C= , CM000676.2:g.20793560C= GRCh38
NC_000014.8:g.21261719C= , CM000676.1:g.21261719C= GRCh37
NC_000014.7:g.20331559C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943584.1:n.585+774C=
XR_943585.1:n.585+774C=
XR_001750620.1:n.3271+774C=
XR_001750621.1:n.3271+774C=
XR_001750622.1:n.637+6344G=
XR_001750623.1:n.637+6344G=
XR_001750624.1:n.637+6344G=