Canonical Allele Identifier: CA730645660
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1452939841
MyVariant Identifiers: chr1:g.207627307G>A (hg19) chr1:g.207453962G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453962G>A , CM000663.2:g.207453962G>A GRCh38
NC_000001.10:g.207627307G>A , CM000663.1:g.207627307G>A GRCh37
NC_000001.9:g.205693930G>A NCBI36
NG_013006.1:g.4663G>A , LRG_348:g.4663G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+867G>A ENSP00000514493.1:n.-385+867G>A
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