Canonical Allele Identifier: CA1818161708
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127012540T= , CM000670.2:g.127012540T= GRCh38
NC_000008.10:g.128024785T= , CM000670.1:g.128024785T= GRCh37
NC_000008.9:g.128093967T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1364+5922T=