Canonical Allele Identifier: CA528606220
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs1306388147
gnomAD v2: 1-207627541-C-T
gnomAD v4: 1-207454196-C-T
MyVariant Identifiers: chr1:g.207627541C>T (hg19) chr1:g.207454196C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454196C>T , CM000663.2:g.207454196C>T GRCh38
NC_000001.10:g.207627541C>T , CM000663.1:g.207627541C>T GRCh37
NC_000001.9:g.205694164C>T NCBI36
NG_013006.1:g.4897C>T , LRG_348:g.4897C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1101C>T ENSP00000514493.1:n.-385+1101C>T
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