Canonical Allele Identifier: CA36635078
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1024750932
MyVariant Identifiers: chr1:g.207627339C>A (hg19) chr1:g.207453994C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453994C>A , CM000663.2:g.207453994C>A GRCh38
NC_000001.10:g.207627339C>A , CM000663.1:g.207627339C>A GRCh37
NC_000001.9:g.205693962C>A NCBI36
NG_013006.1:g.4695C>A , LRG_348:g.4695C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+899C>A ENSP00000514493.1:n.-385+899C>A
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