Canonical Allele Identifier: CA2137107148
Gene:

Linked Data

dbSNP Id: rs2034713836

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417670A>C , CM000676.2:g.52417670A>C GRCh38
NC_000014.8:g.52884388A>C , CM000676.1:g.52884388A>C GRCh37
NC_000014.7:g.51954138A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3033T>G