Canonical Allele Identifier: CA2720283648
Gene:

Linked Data

dbSNP Id: rs2118594221

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.108092922A>C , CM000671.2:g.108092922A>C GRCh38
NC_000009.11:g.110855203A>C , CM000671.1:g.110855203A>C GRCh37
NC_000009.10:g.109895024A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930239.1:n.461-39628T>G
XR_001746881.1:n.668-39628T>G
XR_001746882.1:n.668-39628T>G