Canonical Allele Identifier: CA363507492

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007963T>G (hg19) ; chr6:g.32040186T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040186T>G , CM000668.2:g.32040186T>G	GRCh38
NC_000006.11:g.32007963T>G , CM000668.1:g.32007963T>G	GRCh37
NC_000006.10:g.32115942T>G	NCBI36
NG_007941.2:g.6879T>G
NG_008337.2:g.74189A>C
NG_007941.3:g.6882T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.920T>G MANE Select	ENSP00000496625.1:p.Phe307Cys
ENST00000418967.6:c.920T>G	ENSP00000408860.2:p.Phe307Cys
ENST00000435122.3:c.830T>G	ENSP00000415043.2:p.Phe277Cys
ENST00000479074.5:n.978T>G
ENST00000479730.5:n.1036T>G
ENST00000483041.5:n.1089T>G
ENST00000486063.5:n.919-220T>G
NM_000500.7:c.920T>G	NP_000491.4:p.Phe307Cys
NM_001128590.3:c.830T>G	NP_001122062.3:p.Phe277Cys
XM_011514314.1:c.515T>G	XP_011512616.1:p.Phe172Cys
NM_000500.9:c.920T>G MANE Select	NP_000491.4:p.Phe307Cys
NM_001368143.1:c.515T>G	NP_001355072.1:p.Phe172Cys
NM_001368144.1:c.515T>G	NP_001355073.1:p.Phe172Cys
NM_001128590.4:c.830T>G	NP_001122062.3:p.Phe277Cys
NM_001368143.2:c.515T>G	NP_001355072.1:p.Phe172Cys
NM_001368144.2:c.515T>G	NP_001355073.1:p.Phe172Cys