Canonical Allele Identifier: CA427349455
Gene:

Linked Data

dbSNP Id: rs564137264
MyVariant Identifiers: chr2:g.88315916G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016397G>C , CM000664.2:g.88016397G>C GRCh38
NC_000002.11:g.88315916G>C , CM000664.1:g.88315916G>C GRCh37
NC_000002.10:g.88097031G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.742G>C
XR_940336.3:n.742G>C