Canonical Allele Identifier: CA15790465
Gene:

Genomic Alleles

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

Transcript Alleles

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