Canonical Allele Identifier: CA43254731

Gene:

Linked Data

• dbSNP Id: rs755670820
• gnomAD v2: 2-16639455-G-A
• gnomAD v3: 2-16458187-G-A
• gnomAD v4: 2-16458187-G-A
• MyVariant Identifiers: chr2:g.16639455G>A (hg19) ; chr2:g.16458187G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.16458187G>A , CM000664.2:g.16458187G>A	GRCh38
NC_000002.11:g.16639455G>A , CM000664.1:g.16639455G>A	GRCh37
NC_000002.10:g.16502936G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939752.1:n.396-3093C>T