Canonical Allele Identifier: CA43588683

Gene:

Linked Data

• dbSNP Id: rs933811158
• MyVariant Identifiers: chr2:g.18025357G>A (hg19) ; chr2:g.17844090G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.17844090G>A , CM000664.2:g.17844090G>A	GRCh38
NC_000002.11:g.18025357G>A , CM000664.1:g.18025357G>A	GRCh37
NC_000002.10:g.17888838G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_939764.2:n.447+3604C>T