Canonical Allele Identifier: CA1818161747
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127012569T= , CM000670.2:g.127012569T= GRCh38
NC_000008.10:g.128024814T= , CM000670.1:g.128024814T= GRCh37
NC_000008.9:g.128093996T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1364+5951T=