Canonical Allele Identifier: CA425902292
Gene:

Linked Data

dbSNP Id: rs1183884720
MyVariant Identifiers: chr2:g.52949598G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722460G>C , CM000664.2:g.52722460G>C GRCh38
NC_000002.11:g.52949598G>C , CM000664.1:g.52949598G>C GRCh37
NC_000002.10:g.52803102G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.797C>G