Canonical Allele Identifier: CA154393467

Gene:

Linked Data

• dbSNP Id: rs780359719
• gnomAD v2: 7-13440202-A-C
• gnomAD v3: 7-13400577-A-C
• gnomAD v4: 7-13400577-A-C
• MyVariant Identifiers: chr7:g.13440202A>C (hg19) ; chr7:g.13400577A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.13400577A>C , CM000669.2:g.13400577A>C	GRCh38
NC_000007.13:g.13440202A>C , CM000669.1:g.13440202A>C	GRCh37
NC_000007.12:g.13406727A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745097.1:n.147+90254A>C