Canonical Allele Identifier: CA449819137
Gene: CYP21A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32008647T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32040870T>C , CM000668.2:g.32040870T>C GRCh38
NC_000006.11:g.32008647T>C , CM000668.1:g.32008647T>C GRCh37
NC_000006.10:g.32116626T>C NCBI36
NG_007941.2:g.7563T>C
NG_008337.2:g.73505A>G
NG_007941.3:g.7566T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.1224T>C MANE Select ENSP00000496625.1:p.Asp408=
ENST00000418967.6:c.1224T>C ENSP00000408860.2:p.Asp408=
ENST00000435122.3:c.1134T>C ENSP00000415043.2:p.Asp378=
ENST00000479074.5:n.1365T>C
ENST00000479730.5:n.1340T>C
ENST00000483041.5:n.1393T>C
ENST00000486063.5:n.1203T>C
NM_000500.7:c.1224T>C NP_000491.4:p.Asp408=
NM_001128590.3:c.1134T>C NP_001122062.3:p.Asp378=
XM_011514314.1:c.819T>C XP_011512616.1:p.Asp273=
NM_000500.9:c.1224T>C MANE Select NP_000491.4:p.Asp408=
NM_001368143.1:c.819T>C NP_001355072.1:p.Asp273=
NM_001368144.1:c.819T>C NP_001355073.1:p.Asp273=
NM_001128590.4:c.1134T>C NP_001122062.3:p.Asp378=
NM_001368143.2:c.819T>C NP_001355072.1:p.Asp273=
NM_001368144.2:c.819T>C NP_001355073.1:p.Asp273=