Canonical Allele Identifier: CA36635170

Gene: CR2

Linked Data

• dbSNP Id: rs969188507
• gnomAD v2: 1-207627536-C-A
• gnomAD v3: 1-207454191-C-A
• gnomAD v4: 1-207454191-C-A
• MyVariant Identifiers: chr1:g.207627536C>A (hg19) ; chr1:g.207454191C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454191C>A , CM000663.2:g.207454191C>A	GRCh38
NC_000001.10:g.207627536C>A , CM000663.1:g.207627536C>A	GRCh37
NC_000001.9:g.205694159C>A	NCBI36
NG_013006.1:g.4892C>A , LRG_348:g.4892C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699640.1:c.-385+1096C>A	ENSP00000514493.1:n.-385+1096C>A