Canonical Allele Identifier: CA1011643164
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1572942048
gnomAD v3: 1-207454192-A-C
gnomAD v4: 1-207454192-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454192A>C , CM000663.2:g.207454192A>C GRCh38
NC_000001.10:g.207627537A>C , CM000663.1:g.207627537A>C GRCh37
NC_000001.9:g.205694160A>C NCBI36
NG_013006.1:g.4893A>C , LRG_348:g.4893A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1097A>C ENSP00000514493.1:n.-385+1097A>C
Search 100 bp 5'
Search 100 bp 3'