Canonical Allele Identifier: CA36635083
Gene: CR2 HGNC NCBI

Linked Data

dbSNP Id: rs903622224
MyVariant Identifiers: chr1:g.207627350T>C (hg19) chr1:g.207454005T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207454005T>C , CM000663.2:g.207454005T>C GRCh38
NC_000001.10:g.207627350T>C , CM000663.1:g.207627350T>C GRCh37
NC_000001.9:g.205693973T>C NCBI36
NG_013006.1:g.4706T>C , LRG_348:g.4706T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699640.1:c.-385+910T>C ENSP00000514493.1:n.-385+910T>C
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