Canonical Allele Identifier: CA597652479
Gene: CYP2R1 HGNC NCBI

Linked Data

dbSNP Id: rs1555017960
gnomAD v2: 11-14915573-A-C
gnomAD v3: 11-14894027-A-C
gnomAD v4: 11-14894027-A-C
MyVariant Identifiers: chr11:g.14915573A>C (hg19) chr11:g.14894027A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14894027A>C , CM000673.2:g.14894027A>C GRCh38
NC_000011.9:g.14915573A>C , CM000673.1:g.14915573A>C GRCh37
NC_000011.8:g.14872149A>C NCBI36
NG_007936.1:g.3179T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011519898.1:c.-1783T>G XP_011518200.1:n.-1783T>G
XM_011519898.3:c.-1783T>G XP_011518200.1:n.-1783T>G
Search 100 bp 5'
Search 100 bp 3'