Canonical Allele Identifier: CA756174376

Gene:

Linked Data

• dbSNP Id: rs1250187310
• MyVariant Identifiers: chr2:g.123126536G>A (hg19) ; chr2:g.122368960G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122368960G>A , CM000664.2:g.122368960G>A	GRCh38
NC_000002.11:g.123126536G>A , CM000664.1:g.123126536G>A	GRCh37
NC_000002.10:g.122843006G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923278.1:n.556-24003G>A
XR_001739684.1:n.556-24003G>A