Canonical Allele Identifier: CA54579345

Gene:

Linked Data

• dbSNP Id: rs564754975
• gnomAD v2: 2-118837357-C-T
• gnomAD v3: 2-118079781-C-T
• gnomAD v4: 2-118079781-C-T
• MyVariant Identifiers: chr2:g.118837357C>T (hg19) ; chr2:g.118079781C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118079781C>T , CM000664.2:g.118079781C>T	GRCh38
NC_000002.11:g.118837357C>T , CM000664.1:g.118837357C>T	GRCh37
NC_000002.10:g.118553827C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011512305.1:c.697-2249G>A	XP_011510607.1:n.697-2249G>A
XR_001739662.2:n.138+8470G>A