Canonical Allele Identifier: CA2137107053
Gene:

Linked Data

dbSNP Id: rs2034712856

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417591G>T , CM000676.2:g.52417591G>T GRCh38
NC_000014.8:g.52884309G>T , CM000676.1:g.52884309G>T GRCh37
NC_000014.7:g.51954059G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3112C>A