Canonical Allele Identifier: CA55081999

Gene:

Linked Data

• dbSNP Id: rs563491476
• MyVariant Identifiers: chr2:g.123641434G>A (hg19) ; chr2:g.122883858G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122883858G>A , CM000664.2:g.122883858G>A	GRCh38
NC_000002.11:g.123641434G>A , CM000664.1:g.123641434G>A	GRCh37
NC_000002.10:g.123357904G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923292.1:n.1125-1084G>A
XR_001739692.1:n.1451-1084G>A
XR_923292.2:n.1358-1084G>A