Canonical Allele Identifier: CA1619399386
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32040757A= , CM000668.2:g.32040757A= GRCh38
NC_000006.11:g.32008534A= , CM000668.1:g.32008534A= GRCh37
NC_000006.10:g.32116513A= NCBI36
NG_007941.2:g.7450A=
NG_008337.2:g.73618T=
NG_007941.3:g.7453A=

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.1208A= MANE Select ENSP00000496625.1:p.His403=
ENST00000418967.6:c.1208A= ENSP00000408860.2:p.His403=
ENST00000435122.3:c.1118A= ENSP00000415043.2:p.His373=
ENST00000479074.5:n.1349A=
ENST00000479730.5:n.1324A=
ENST00000483041.5:n.1377A=
ENST00000486063.5:n.1187A=
NM_000500.7:c.1208A= NP_000491.4:p.His403=
NM_001128590.3:c.1118A= NP_001122062.3:p.His373=
XM_011514314.1:c.803A= XP_011512616.1:p.His268=
NM_000500.9:c.1208A= MANE Select NP_000491.4:p.His403=
NM_001368143.1:c.803A= NP_001355072.1:p.His268=
NM_001368144.1:c.803A= NP_001355073.1:p.His268=
NM_001128590.4:c.1118A= NP_001122062.3:p.His373=
NM_001368143.2:c.803A= NP_001355072.1:p.His268=
NM_001368144.2:c.803A= NP_001355073.1:p.His268=