Canonical Allele Identifier: CA449729161

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007141A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039364A>G , CM000668.2:g.32039364A>G	GRCh38
NC_000006.11:g.32007141A>G , CM000668.1:g.32007141A>G	GRCh37
NC_000006.10:g.32115120A>G	NCBI36
NG_007941.2:g.6057A>G
NG_008337.2:g.75011T>C
NG_007941.3:g.6060A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.456A>G MANE Select	ENSP00000496625.1:p.Arg152=
ENST00000418967.6:c.456A>G	ENSP00000408860.2:p.Arg152=
ENST00000435122.3:c.366A>G	ENSP00000415043.2:p.Arg122=
ENST00000462278.1:n.44A>G
ENST00000464325.5:n.377A>G
ENST00000466779.5:c.*148A>G	ENSP00000417321.1:n.*148A>G
ENST00000466879.5:n.507A>G
ENST00000469053.5:c.*148A>G	ENSP00000418104.1:n.*148A>G
ENST00000471671.4:c.456A>G	ENSP00000418561.1:p.Arg152=
ENST00000478281.5:c.489A>G	ENSP00000419572.1:p.Arg163=
ENST00000479074.5:n.514A>G
ENST00000479730.5:n.611A>G
ENST00000483041.5:n.625A>G
ENST00000486063.5:n.636A>G
ENST00000488465.1:n.464A>G
NM_000500.7:c.456A>G	NP_000491.4:p.Arg152=
NM_001128590.3:c.366A>G	NP_001122062.3:p.Arg122=
XM_011514314.1:c.51A>G	XP_011512616.1:p.Arg17=
NM_000500.9:c.456A>G MANE Select	NP_000491.4:p.Arg152=
NM_001368143.1:c.51A>G	NP_001355072.1:p.Arg17=
NM_001368144.1:c.51A>G	NP_001355073.1:p.Arg17=
NM_001128590.4:c.366A>G	NP_001122062.3:p.Arg122=
NM_001368143.2:c.51A>G	NP_001355072.1:p.Arg17=
NM_001368144.2:c.51A>G	NP_001355073.1:p.Arg17=