Canonical Allele Identifier: CA2697928408
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs2102291728
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454171G>A , CM000663.2:g.207454171G>A GRCh38
NC_000001.10:g.207627516G>A , CM000663.1:g.207627516G>A GRCh37
NC_000001.9:g.205694139G>A NCBI36
NG_013006.1:g.4872G>A , LRG_348:g.4872G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000699640.1:c.-385+1076G>A ENSP00000514493.1:n.-385+1076G>A
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