Canonical Allele Identifier: CA36634992
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs944980345
MyVariant Identifiers: chr1:g.207627191A>G (hg19) chr1:g.207453846A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207453846A>G , CM000663.2:g.207453846A>G GRCh38
NC_000001.10:g.207627191A>G , CM000663.1:g.207627191A>G GRCh37
NC_000001.9:g.205693814A>G NCBI36
NG_013006.1:g.4547A>G , LRG_348:g.4547A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+751A>G ENSP00000514493.1:n.-385+751A>G
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