Canonical Allele Identifier: CA2527505219
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079722C>A , CM000664.2:g.118079722C>A GRCh38
NC_000002.11:g.118837298C>A , CM000664.1:g.118837298C>A GRCh37
NC_000002.10:g.118553768C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512305.1:c.697-2190G>T XP_011510607.1:n.697-2190G>T
XR_001739662.2:n.138+8529G>T