Canonical Allele Identifier: CA427349487

Gene:

Linked Data

• dbSNP Id: rs78243397
• gnomAD v3: 2-88016415-A-T
• gnomAD v4: 2-88016415-A-T
• MyVariant Identifiers: chr2:g.88315934A>T (hg19) ; chr2:g.88016415A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016415A>T , CM000664.2:g.88016415A>T	GRCh38
NC_000002.11:g.88315934A>T , CM000664.1:g.88315934A>T	GRCh37
NC_000002.10:g.88097049A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.760A>T
XR_940336.3:n.760A>T