Canonical Allele Identifier: CA597652523
Gene: CYP2R1 HGNC NCBI

Linked Data

dbSNP Id: rs1555018000
gnomAD v2: 11-14915819-T-C
gnomAD v3: 11-14894273-T-C
gnomAD v4: 11-14894273-T-C
MyVariant Identifiers: chr11:g.14915819T>C (hg19) chr11:g.14894273T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14894273T>C , CM000673.2:g.14894273T>C GRCh38
NC_000011.9:g.14915819T>C , CM000673.1:g.14915819T>C GRCh37
NC_000011.8:g.14872395T>C NCBI36
NG_007936.1:g.2933A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011519898.3:c.-2029A>G XP_011518200.1:n.-2029A>G
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