Canonical Allele Identifier: CA1758346762
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2923373C= , CM000670.2:g.2923373C= GRCh38
NC_000008.10:g.2780895C= , CM000670.1:g.2780895C= GRCh37
NC_000008.9:g.2768302C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941365.1:n.127+189G=
XR_941367.1:n.212-2392C=
XR_002956657.1:n.1002-2392C=
XR_002956658.1:n.3030-2392C=
NR_168441.1:n.1167-77632C=
NR_168442.1:n.1698-2392C=
NR_168443.1:n.1172-85195C=
NR_168444.1:n.1167-66165C=
NR_168445.1:n.1250-66165C=