Canonical Allele Identifier: CA893591024
Gene:

Linked Data

dbSNP Id: rs1352764993
MyVariant Identifiers: chr2:g.81872960G>A (hg19) chr2:g.81645836G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.81645836G>A , CM000664.2:g.81645836G>A GRCh38
NC_000002.11:g.81872960G>A , CM000664.1:g.81872960G>A GRCh37
NC_000002.10:g.81726471G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940294.1:n.563+66227G>A
XR_940295.1:n.485+97089G>A
XR_001739571.1:n.485+97089G>A
Search 100 bp 5'
Search 100 bp 3'