Canonical Allele Identifier: CA534498816
Gene:

Linked Data

dbSNP Id: rs1351829777
gnomAD v2: 2-88315490-C-G
MyVariant Identifiers: chr2:g.88315490C>G (hg19) chr2:g.88015971C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88015971C>G , CM000664.2:g.88015971C>G GRCh38
NC_000002.11:g.88315490C>G , CM000664.1:g.88315490C>G GRCh37
NC_000002.10:g.88096605C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.316C>G
XR_940336.3:n.316C>G
Search 100 bp 5'
Search 100 bp 3'