Canonical Allele Identifier: CA36635001
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs903369678
gnomAD v3: 1-207453863-A-G
gnomAD v4: 1-207453863-A-G
MyVariant Identifiers: chr1:g.207627208A>G (hg19) chr1:g.207453863A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453863A>G , CM000663.2:g.207453863A>G GRCh38
NC_000001.10:g.207627208A>G , CM000663.1:g.207627208A>G GRCh37
NC_000001.9:g.205693831A>G NCBI36
NG_013006.1:g.4564A>G , LRG_348:g.4564A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+768A>G ENSP00000514493.1:n.-385+768A>G
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