Canonical Allele Identifier: CA2606980700
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs2102291436
gnomAD v3: 1-207453904-T-C
gnomAD v4: 1-207453904-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453904T>C , CM000663.2:g.207453904T>C GRCh38
NC_000001.10:g.207627249T>C , CM000663.1:g.207627249T>C GRCh37
NC_000001.9:g.205693872T>C NCBI36
NG_013006.1:g.4605T>C , LRG_348:g.4605T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+809T>C ENSP00000514493.1:n.-385+809T>C
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Search 100 bp 3'