Canonical Allele Identifier: CA449818709

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007382C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039605C>T , CM000668.2:g.32039605C>T	GRCh38
NC_000006.11:g.32007382C>T , CM000668.1:g.32007382C>T	GRCh37
NC_000006.10:g.32115361C>T	NCBI36
NG_007941.2:g.6298C>T
NG_008337.2:g.74770G>A
NG_007941.3:g.6301C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.609C>T MANE Select	ENSP00000496625.1:p.Ser203=
ENST00000418967.6:c.609C>T	ENSP00000408860.2:p.Ser203=
ENST00000435122.3:c.519C>T	ENSP00000415043.2:p.Ser173=
ENST00000462278.1:n.197C>T
ENST00000464325.5:n.530C>T
ENST00000466779.5:c.*301C>T	ENSP00000417321.1:n.*301C>T
ENST00000466879.5:n.660C>T
ENST00000469053.5:c.*301C>T	ENSP00000418104.1:n.*301C>T
ENST00000471671.4:c.570C>T	ENSP00000418561.1:p.Ser190=
ENST00000479074.5:n.667C>T
ENST00000479730.5:n.725C>T
ENST00000483041.5:n.778C>T
ENST00000486063.5:n.789C>T
NM_000500.7:c.609C>T	NP_000491.4:p.Ser203=
NM_001128590.3:c.519C>T	NP_001122062.3:p.Ser173=
XM_011514314.1:c.204C>T	XP_011512616.1:p.Ser68=
NM_000500.9:c.609C>T MANE Select	NP_000491.4:p.Ser203=
NM_001368143.1:c.204C>T	NP_001355072.1:p.Ser68=
NM_001368144.1:c.204C>T	NP_001355073.1:p.Ser68=
NM_001128590.4:c.519C>T	NP_001122062.3:p.Ser173=
NM_001368143.2:c.204C>T	NP_001355072.1:p.Ser68=
NM_001368144.2:c.204C>T	NP_001355073.1:p.Ser68=