Canonical Allele Identifier: CA756214899
Gene:

Linked Data

dbSNP Id: rs1292539516
MyVariant Identifiers: chr2:g.123641449A>G (hg19) chr2:g.122883873A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883873A>G , CM000664.2:g.122883873A>G GRCh38
NC_000002.11:g.123641449A>G , CM000664.1:g.123641449A>G GRCh37
NC_000002.10:g.123357919A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-1069A>G
XR_001739692.1:n.1451-1069A>G
XR_923292.2:n.1358-1069A>G
Search 100 bp 5'
Search 100 bp 3'