Canonical Allele Identifier: CA363507169
Gene: CYP21A2 HGNC NCBI

Linked Data

gnomAD v4: 6-32040146-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32040146A>G , CM000668.2:g.32040146A>G GRCh38
NC_000006.11:g.32007923A>G , CM000668.1:g.32007923A>G GRCh37
NC_000006.10:g.32115902A>G NCBI36
NG_007941.2:g.6839A>G
NG_008337.2:g.74229T>C
NG_007941.3:g.6842A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.880A>G MANE Select ENSP00000496625.1:p.Thr294Ala
ENST00000418967.6:c.880A>G ENSP00000408860.2:p.Thr294Ala
ENST00000435122.3:c.790A>G ENSP00000415043.2:p.Thr264Ala
ENST00000479074.5:n.938A>G
ENST00000479730.5:n.996A>G
ENST00000483041.5:n.1049A>G
ENST00000486063.5:n.919-260A>G
NM_000500.7:c.880A>G NP_000491.4:p.Thr294Ala
NM_001128590.3:c.790A>G NP_001122062.3:p.Thr264Ala
XM_011514314.1:c.475A>G XP_011512616.1:p.Thr159Ala
NM_000500.9:c.880A>G MANE Select NP_000491.4:p.Thr294Ala
NM_001368143.1:c.475A>G NP_001355072.1:p.Thr159Ala
NM_001368144.1:c.475A>G NP_001355073.1:p.Thr159Ala
NM_001128590.4:c.790A>G NP_001122062.3:p.Thr264Ala
NM_001368143.2:c.475A>G NP_001355072.1:p.Thr159Ala
NM_001368144.2:c.475A>G NP_001355073.1:p.Thr159Ala