Canonical Allele Identifier: CA2483404544
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1657768659
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454274C>G , CM000663.2:g.207454274C>G GRCh38
NC_000001.10:g.207627619C>G , CM000663.1:g.207627619C>G GRCh37
NC_000001.9:g.205694242C>G NCBI36
NG_013006.1:g.4975C>G , LRG_348:g.4975C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000699640.1:c.-385+1179C>G ENSP00000514493.1:n.-385+1179C>G
ENST00000367057.7:c.-145C>G ENSP00000356024.3:n.-145C>G
ENST00000367058.7:c.-145C>G ENSP00000356025.3:n.-145C>G
ENST00000367059.3:c.-145C>G ENSP00000356026.3:n.-145C>G
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