Canonical Allele Identifier: CA892287837
Gene:

Linked Data

dbSNP Id: rs1346989490
MyVariant Identifiers: chr2:g.67864613A>G (hg19) chr2:g.67637481A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.67637481A>G , CM000664.2:g.67637481A>G GRCh38
NC_000002.11:g.67864613A>G , CM000664.1:g.67864613A>G GRCh37
NC_000002.10:g.67718117A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739524.1:n.65+13485T>C
Search 100 bp 5'
Search 100 bp 3'