Canonical Allele Identifier: CA2538789488
Gene: CR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453970C>A , CM000663.2:g.207453970C>A GRCh38
NC_000001.10:g.207627315C>A , CM000663.1:g.207627315C>A GRCh37
NC_000001.9:g.205693938C>A NCBI36
NG_013006.1:g.4671C>A , LRG_348:g.4671C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+875C>A ENSP00000514493.1:n.-385+875C>A
Search 100 bp 5'
Search 100 bp 3'