Canonical Allele Identifier: CA449729819

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007934A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040157A>G , CM000668.2:g.32040157A>G	GRCh38
NC_000006.11:g.32007934A>G , CM000668.1:g.32007934A>G	GRCh37
NC_000006.10:g.32115913A>G	NCBI36
NG_007941.2:g.6850A>G
NG_008337.2:g.74218T>C
NG_007941.3:g.6853A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.891A>G MANE Select	ENSP00000496625.1:p.Thr297=
ENST00000418967.6:c.891A>G	ENSP00000408860.2:p.Thr297=
ENST00000435122.3:c.801A>G	ENSP00000415043.2:p.Thr267=
ENST00000479074.5:n.949A>G
ENST00000479730.5:n.1007A>G
ENST00000483041.5:n.1060A>G
ENST00000486063.5:n.919-249A>G
NM_000500.7:c.891A>G	NP_000491.4:p.Thr297=
NM_001128590.3:c.801A>G	NP_001122062.3:p.Thr267=
XM_011514314.1:c.486A>G	XP_011512616.1:p.Thr162=
NM_000500.9:c.891A>G MANE Select	NP_000491.4:p.Thr297=
NM_001368143.1:c.486A>G	NP_001355072.1:p.Thr162=
NM_001368144.1:c.486A>G	NP_001355073.1:p.Thr162=
NM_001128590.4:c.801A>G	NP_001122062.3:p.Thr267=
NM_001368143.2:c.486A>G	NP_001355072.1:p.Thr162=
NM_001368144.2:c.486A>G	NP_001355073.1:p.Thr162=