Canonical Allele Identifier: CA36635034
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs889248244
gnomAD v3: 1-207453942-T-C
gnomAD v4: 1-207453942-T-C
MyVariant Identifiers: chr1:g.207627287T>C (hg19) chr1:g.207453942T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453942T>C , CM000663.2:g.207453942T>C GRCh38
NC_000001.10:g.207627287T>C , CM000663.1:g.207627287T>C GRCh37
NC_000001.9:g.205693910T>C NCBI36
NG_013006.1:g.4643T>C , LRG_348:g.4643T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+847T>C ENSP00000514493.1:n.-385+847T>C
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