Canonical Allele Identifier: CA730645822

Gene: CR2

Linked Data

• dbSNP Id: rs1217704130
• MyVariant Identifiers: chr1:g.207627558C>T (hg19) ; chr1:g.207454213C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454213C>T , CM000663.2:g.207454213C>T	GRCh38
NC_000001.10:g.207627558C>T , CM000663.1:g.207627558C>T	GRCh37
NC_000001.9:g.205694181C>T	NCBI36
NG_013006.1:g.4914C>T , LRG_348:g.4914C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699640.1:c.-385+1118C>T	ENSP00000514493.1:n.-385+1118C>T