Canonical Allele Identifier: CA36635147
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs756386382
MyVariant Identifiers: chr1:g.207627511_207627512del (hg19) chr1:g.207454166_207454167del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454167_207454168del , CM000663.2:g.207454167_207454168del GRCh38
NC_000001.10:g.207627512_207627513del , CM000663.1:g.207627512_207627513del GRCh37
NC_000001.9:g.205694135_205694136del NCBI36
NG_013006.1:g.4868_4869del , LRG_348:g.4868_4869del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1072_-385+1073del ENSP00000514493.1:n.-385+1072_-385+1073del
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