Canonical Allele Identifier: CA756215016

Gene:

Linked Data

• dbSNP Id: rs1370457619
• MyVariant Identifiers: chr2:g.123641694G>A (hg19) ; chr2:g.122884118G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122884118G>A , CM000664.2:g.122884118G>A	GRCh38
NC_000002.11:g.123641694G>A , CM000664.1:g.123641694G>A	GRCh37
NC_000002.10:g.123358164G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923292.1:n.1125-824G>A
XR_001739692.1:n.1451-824G>A
XR_923292.2:n.1358-824G>A