Canonical Allele Identifier: CA36634993
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1041963015
MyVariant Identifiers: chr1:g.207627201_207627204del (hg19) chr1:g.207453856_207453859del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453858_207453861del , CM000663.2:g.207453858_207453861del GRCh38
NC_000001.10:g.207627203_207627206del , CM000663.1:g.207627203_207627206del GRCh37
NC_000001.9:g.205693826_205693829del NCBI36
NG_013006.1:g.4559_4562del , LRG_348:g.4559_4562del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+763_-385+766del ENSP00000514493.1:n.-385+763_-385+766del
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