Canonical Allele Identifier: CA730645708

Gene: CR2

Linked Data

• dbSNP Id: rs1372444693
• gnomAD v3: 1-207454062-T-C
• gnomAD v4: 1-207454062-T-C
• MyVariant Identifiers: chr1:g.207627407T>C (hg19) ; chr1:g.207454062T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454062T>C , CM000663.2:g.207454062T>C	GRCh38
NC_000001.10:g.207627407T>C , CM000663.1:g.207627407T>C	GRCh37
NC_000001.9:g.205694030T>C	NCBI36
NG_013006.1:g.4763T>C , LRG_348:g.4763T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699640.1:c.-385+967T>C	ENSP00000514493.1:n.-385+967T>C