Canonical Allele Identifier: CA2302316774
Gene:

Linked Data

dbSNP Id: rs1568552075

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645831T>A , CM000680.2:g.49645831T>A GRCh38
NC_000018.9:g.47172201T>A , CM000680.1:g.47172201T>A GRCh37
NC_000018.8:g.45426199T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935461.1:n.162-16203T>A
XR_001753446.1:n.898-16203T>A