Canonical Allele Identifier: CA449818454

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32006527C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038750C>G , CM000668.2:g.32038750C>G	GRCh38
NC_000006.11:g.32006527C>G , CM000668.1:g.32006527C>G	GRCh37
NC_000006.10:g.32114506C>G	NCBI36
NG_007941.2:g.5443C>G
NG_007941.3:g.5446C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.231C>G MANE Select	ENSP00000496625.1:p.Thr77=
ENST00000418967.6:c.231C>G	ENSP00000408860.2:p.Thr77=
ENST00000435122.3:c.202+126C>G	ENSP00000415043.2:n.202+126C>G
ENST00000464325.5:n.168C>G
ENST00000466779.5:c.231C>G	ENSP00000417321.1:p.Thr77=
ENST00000469053.5:c.202+126C>G	ENSP00000418104.1:n.202+126C>G
ENST00000471671.4:c.231C>G	ENSP00000418561.1:p.Thr77=
ENST00000478281.5:c.231C>G	ENSP00000419572.1:p.Thr77=
ENST00000479074.5:n.289C>G
ENST00000479730.5:n.386C>G
ENST00000480027.1:n.284C>G
ENST00000483041.5:n.381C>G
ENST00000486063.5:n.411C>G
ENST00000488465.1:n.239C>G
NM_000500.7:c.231C>G	NP_000491.4:p.Thr77=
NM_001128590.3:c.202+126C>G	NP_001122062.3:n.202+126C>G
XM_011514314.1:c.-194C>G	XP_011512616.1:n.-194C>G
NM_000500.9:c.231C>G MANE Select	NP_000491.4:p.Thr77=
NM_001368143.1:c.-194C>G	NP_001355072.1:n.-194C>G
NM_001368144.1:c.-133+126C>G	NP_001355073.1:n.-133+126C>G
NM_001128590.4:c.202+126C>G	NP_001122062.3:n.202+126C>G
NM_001368143.2:c.-194C>G	NP_001355072.1:n.-194C>G
NM_001368144.2:c.-133+126C>G	NP_001355073.1:n.-133+126C>G