Canonical Allele Identifier: CA2137107129
Gene:

Linked Data

dbSNP Id: rs1310821028

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417658T>G , CM000676.2:g.52417658T>G GRCh38
NC_000014.8:g.52884376T>G , CM000676.1:g.52884376T>G GRCh37
NC_000014.7:g.51954126T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3045A>C