Canonical Allele Identifier: CA449818774

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008263T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040486T>G , CM000668.2:g.32040486T>G	GRCh38
NC_000006.11:g.32008263T>G , CM000668.1:g.32008263T>G	GRCh37
NC_000006.10:g.32116242T>G	NCBI36
NG_007941.2:g.7179T>G
NG_008337.2:g.73889A>C
NG_007941.3:g.7182T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1020T>G MANE Select	ENSP00000496625.1:p.Arg340=
ENST00000418967.6:c.1020T>G	ENSP00000408860.2:p.Arg340=
ENST00000435122.3:c.930T>G	ENSP00000415043.2:p.Arg310=
ENST00000479074.5:n.1078T>G
ENST00000479730.5:n.1136T>G
ENST00000483041.5:n.1189T>G
ENST00000486063.5:n.999T>G
NM_000500.7:c.1020T>G	NP_000491.4:p.Arg340=
NM_001128590.3:c.930T>G	NP_001122062.3:p.Arg310=
XM_011514314.1:c.615T>G	XP_011512616.1:p.Arg205=
NM_000500.9:c.1020T>G MANE Select	NP_000491.4:p.Arg340=
NM_001368143.1:c.615T>G	NP_001355072.1:p.Arg205=
NM_001368144.1:c.615T>G	NP_001355073.1:p.Arg205=
NM_001128590.4:c.930T>G	NP_001122062.3:p.Arg310=
NM_001368143.2:c.615T>G	NP_001355072.1:p.Arg205=
NM_001368144.2:c.615T>G	NP_001355073.1:p.Arg205=