Canonical Allele Identifier: CA833583468

Gene:

Linked Data

• dbSNP Id: rs1472345096
• gnomAD v3: 7-13400631-C-G
• gnomAD v4: 7-13400631-C-G
• MyVariant Identifiers: chr7:g.13440256C>G (hg19) ; chr7:g.13400631C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.13400631C>G , CM000669.2:g.13400631C>G	GRCh38
NC_000007.13:g.13440256C>G , CM000669.1:g.13440256C>G	GRCh37
NC_000007.12:g.13406781C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001745097.1:n.147+90308C>G