Canonical Allele Identifier: CA2483404487
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs969188507
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Genomic Alleles

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

Transcript Alleles

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