Canonical Allele Identifier: CA2137107055
Gene:

Linked Data

dbSNP Id: rs2034712876

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417592G>C , CM000676.2:g.52417592G>C GRCh38
NC_000014.8:g.52884310G>C , CM000676.1:g.52884310G>C GRCh37
NC_000014.7:g.51954060G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3111C>G