Canonical Allele Identifier: CA363504269

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007412T>G (hg19) ; chr6:g.32039635T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039635T>G , CM000668.2:g.32039635T>G	GRCh38
NC_000006.11:g.32007412T>G , CM000668.1:g.32007412T>G	GRCh37
NC_000006.10:g.32115391T>G	NCBI36
NG_007941.2:g.6328T>G
NG_008337.2:g.74740A>C
NG_007941.3:g.6331T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.639T>G MANE Select	ENSP00000496625.1:p.Ile213Met
ENST00000418967.6:c.639T>G	ENSP00000408860.2:p.Ile213Met
ENST00000435122.3:c.549T>G	ENSP00000415043.2:p.Ile183Met
ENST00000462278.1:n.227T>G
ENST00000464325.5:n.560T>G
ENST00000466779.5:c.*331T>G	ENSP00000417321.1:n.*331T>G
ENST00000466879.5:n.690T>G
ENST00000469053.5:c.*331T>G	ENSP00000418104.1:n.*331T>G
ENST00000479074.5:n.697T>G
ENST00000479730.5:n.755T>G
ENST00000483041.5:n.808T>G
ENST00000486063.5:n.819T>G
NM_000500.7:c.639T>G	NP_000491.4:p.Ile213Met
NM_001128590.3:c.549T>G	NP_001122062.3:p.Ile183Met
XM_011514314.1:c.234T>G	XP_011512616.1:p.Ile78Met
NM_000500.9:c.639T>G MANE Select	NP_000491.4:p.Ile213Met
NM_001368143.1:c.234T>G	NP_001355072.1:p.Ile78Met
NM_001368144.1:c.234T>G	NP_001355073.1:p.Ile78Met
NM_001128590.4:c.549T>G	NP_001122062.3:p.Ile183Met
NM_001368143.2:c.234T>G	NP_001355072.1:p.Ile78Met
NM_001368144.2:c.234T>G	NP_001355073.1:p.Ile78Met