Canonical Allele Identifier: CA363506999

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007900C>T (hg19) ; chr6:g.32040123C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040123C>T , CM000668.2:g.32040123C>T	GRCh38
NC_000006.11:g.32007900C>T , CM000668.1:g.32007900C>T	GRCh37
NC_000006.10:g.32115879C>T	NCBI36
NG_007941.2:g.6816C>T
NG_008337.2:g.74252G>A
NG_007941.3:g.6819C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.857C>T MANE Select	ENSP00000496625.1:p.Ala286Val
ENST00000418967.6:c.857C>T	ENSP00000408860.2:p.Ala286Val
ENST00000435122.3:c.767C>T	ENSP00000415043.2:p.Ala256Val
ENST00000479074.5:n.915C>T
ENST00000479730.5:n.973C>T
ENST00000483041.5:n.1026C>T
ENST00000486063.5:n.919-283C>T
NM_000500.7:c.857C>T	NP_000491.4:p.Ala286Val
NM_001128590.3:c.767C>T	NP_001122062.3:p.Ala256Val
XM_011514314.1:c.452C>T	XP_011512616.1:p.Ala151Val
NM_000500.9:c.857C>T MANE Select	NP_000491.4:p.Ala286Val
NM_001368143.1:c.452C>T	NP_001355072.1:p.Ala151Val
NM_001368144.1:c.452C>T	NP_001355073.1:p.Ala151Val
NM_001128590.4:c.767C>T	NP_001122062.3:p.Ala256Val
NM_001368143.2:c.452C>T	NP_001355072.1:p.Ala151Val
NM_001368144.2:c.452C>T	NP_001355073.1:p.Ala151Val