Canonical Allele Identifier: CA51878391

Gene:

Linked Data

• dbSNP Id: rs531732742
• gnomAD v2: 2-88315918-G-A
• gnomAD v3: 2-88016399-G-A
• gnomAD v4: 2-88016399-G-A
• MyVariant Identifiers: chr2:g.88315918G>A (hg19) ; chr2:g.88016399G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016399G>A , CM000664.2:g.88016399G>A	GRCh38
NC_000002.11:g.88315918G>A , CM000664.1:g.88315918G>A	GRCh37
NC_000002.10:g.88097033G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.744G>A
XR_940336.3:n.744G>A