Canonical Allele Identifier: CA2137107151
Gene:

Linked Data

dbSNP Id: rs1566518822

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417672A>G , CM000676.2:g.52417672A>G GRCh38
NC_000014.8:g.52884390A>G , CM000676.1:g.52884390A>G GRCh37
NC_000014.7:g.51954140A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3031T>C