Canonical Allele Identifier: CA2650261097
Gene: CR2 HGNC NCBI

Linked Data

gnomAD v4: 1-207454153-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454153G>T , CM000663.2:g.207454153G>T GRCh38
NC_000001.10:g.207627498G>T , CM000663.1:g.207627498G>T GRCh37
NC_000001.9:g.205694121G>T NCBI36
NG_013006.1:g.4854G>T , LRG_348:g.4854G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+1058G>T ENSP00000514493.1:n.-385+1058G>T
Search 100 bp 5'
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