Canonical Allele Identifier: CA2699682099
Gene:

Linked Data

dbSNP Id: rs1017879878

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016298G>C , CM000664.2:g.88016298G>C GRCh38
NC_000002.11:g.88315817G>C , CM000664.1:g.88315817G>C GRCh37
NC_000002.10:g.88096932G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.643G>C
XR_940336.3:n.643G>C