Canonical Allele Identifier: CA2770519749

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040398T>G , CM000668.2:g.32040398T>G	GRCh38
NC_000006.11:g.32008175T>G , CM000668.1:g.32008175T>G	GRCh37
NC_000006.10:g.32116154T>G	NCBI36
NG_007941.2:g.7091T>G
NG_008337.2:g.73977A>C
NG_007941.3:g.7094T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.940-8T>G MANE Select	ENSP00000496625.1:n.940-8T>G
ENST00000418967.6:c.940-8T>G	ENSP00000408860.2:n.940-8T>G
ENST00000435122.3:c.850-8T>G	ENSP00000415043.2:n.850-8T>G
ENST00000479074.5:n.998-8T>G
ENST00000479730.5:n.1056-8T>G
ENST00000483041.5:n.1109-8T>G
ENST00000486063.5:n.919-8T>G
NM_000500.7:c.940-8T>G	NP_000491.4:n.940-8T>G
NM_001128590.3:c.850-8T>G	NP_001122062.3:n.850-8T>G
XM_011514314.1:c.535-8T>G	XP_011512616.1:n.535-8T>G
NM_000500.9:c.940-8T>G MANE Select	NP_000491.4:n.940-8T>G
NM_001368143.1:c.535-8T>G	NP_001355072.1:n.535-8T>G
NM_001368144.1:c.535-8T>G	NP_001355073.1:n.535-8T>G
NM_001128590.4:c.850-8T>G	NP_001122062.3:n.850-8T>G
NM_001368143.2:c.535-8T>G	NP_001355072.1:n.535-8T>G
NM_001368144.2:c.535-8T>G	NP_001355073.1:n.535-8T>G