Canonical Allele Identifier: CA363499136

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32006327C>G (hg19) ; chr6:g.32038550C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038550C>G , CM000668.2:g.32038550C>G	GRCh38
NC_000006.11:g.32006327C>G , CM000668.1:g.32006327C>G	GRCh37
NC_000006.10:g.32114306C>G	NCBI36
NG_007941.2:g.5243C>G
NG_007941.3:g.5246C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.128C>G MANE Select	ENSP00000496625.1:p.Pro43Arg
ENST00000418967.6:c.128C>G	ENSP00000408860.2:p.Pro43Arg
ENST00000435122.3:c.128C>G	ENSP00000415043.2:p.Pro43Arg
ENST00000466779.5:c.128C>G	ENSP00000417321.1:p.Pro43Arg
ENST00000469053.5:c.128C>G	ENSP00000418104.1:p.Pro43Arg
ENST00000471671.4:c.128C>G	ENSP00000418561.1:p.Pro43Arg
ENST00000478281.5:c.128C>G	ENSP00000419572.1:p.Pro43Arg
ENST00000479074.5:n.186C>G
ENST00000479730.5:n.186C>G
ENST00000480027.1:n.181C>G
ENST00000483041.5:n.181C>G
ENST00000486063.5:n.211C>G
ENST00000488465.1:n.136C>G
NM_000500.7:c.128C>G	NP_000491.4:p.Pro43Arg
NM_001128590.3:c.128C>G	NP_001122062.3:p.Pro43Arg
XM_011514314.1:c.-297C>G	XP_011512616.1:n.-297C>G
NM_000500.9:c.128C>G MANE Select	NP_000491.4:p.Pro43Arg
NM_001368143.1:c.-297C>G	NP_001355072.1:n.-297C>G
NM_001368144.1:c.-207C>G	NP_001355073.1:n.-207C>G
NM_001128590.4:c.128C>G	NP_001122062.3:p.Pro43Arg
NM_001368143.2:c.-297C>G	NP_001355072.1:n.-297C>G
NM_001368144.2:c.-207C>G	NP_001355073.1:n.-207C>G