Canonical Allele Identifier: CA449729666
Gene: CYP21A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32007865T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32040088T>G , CM000668.2:g.32040088T>G GRCh38
NC_000006.11:g.32007865T>G , CM000668.1:g.32007865T>G GRCh37
NC_000006.10:g.32115844T>G NCBI36
NG_007941.2:g.6781T>G
NG_008337.2:g.74287A>C
NG_007941.3:g.6784T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.822T>G MANE Select ENSP00000496625.1:p.Ser274=
ENST00000418967.6:c.822T>G ENSP00000408860.2:p.Ser274=
ENST00000435122.3:c.732T>G ENSP00000415043.2:p.Ser244=
ENST00000479074.5:n.880T>G
ENST00000479730.5:n.938T>G
ENST00000483041.5:n.991T>G
ENST00000486063.5:n.918+253T>G
NM_000500.7:c.822T>G NP_000491.4:p.Ser274=
NM_001128590.3:c.732T>G NP_001122062.3:p.Ser244=
XM_011514314.1:c.417T>G XP_011512616.1:p.Ser139=
NM_000500.9:c.822T>G MANE Select NP_000491.4:p.Ser274=
NM_001368143.1:c.417T>G NP_001355072.1:p.Ser139=
NM_001368144.1:c.417T>G NP_001355073.1:p.Ser139=
NM_001128590.4:c.732T>G NP_001122062.3:p.Ser244=
NM_001368143.2:c.417T>G NP_001355072.1:p.Ser139=
NM_001368144.2:c.417T>G NP_001355073.1:p.Ser139=