Canonical Allele Identifier: CA2083591000
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.34032049A= , CM000675.2:g.34032049A= GRCh38
NC_000013.10:g.34606186A= , CM000675.1:g.34606186A= GRCh37
NC_000013.9:g.33504186A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001749817.1:n.1515T=