Canonical Allele Identifier: CA363507503

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1329885362
• gnomAD v3: 6-32040187-T-G
• gnomAD v4: 6-32040187-T-G
• MyVariant Identifiers: chr6:g.32007964T>G (hg19) ; chr6:g.32040187T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040187T>G , CM000668.2:g.32040187T>G	GRCh38
NC_000006.11:g.32007964T>G , CM000668.1:g.32007964T>G	GRCh37
NC_000006.10:g.32115943T>G	NCBI36
NG_007941.2:g.6880T>G
NG_008337.2:g.74188A>C
NG_007941.3:g.6883T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.921T>G MANE Select	ENSP00000496625.1:p.Phe307Leu
ENST00000418967.6:c.921T>G	ENSP00000408860.2:p.Phe307Leu
ENST00000435122.3:c.831T>G	ENSP00000415043.2:p.Phe277Leu
ENST00000479074.5:n.979T>G
ENST00000479730.5:n.1037T>G
ENST00000483041.5:n.1090T>G
ENST00000486063.5:n.919-219T>G
NM_000500.7:c.921T>G	NP_000491.4:p.Phe307Leu
NM_001128590.3:c.831T>G	NP_001122062.3:p.Phe277Leu
XM_011514314.1:c.516T>G	XP_011512616.1:p.Phe172Leu
NM_000500.9:c.921T>G MANE Select	NP_000491.4:p.Phe307Leu
NM_001368143.1:c.516T>G	NP_001355072.1:p.Phe172Leu
NM_001368144.1:c.516T>G	NP_001355073.1:p.Phe172Leu
NM_001128590.4:c.831T>G	NP_001122062.3:p.Phe277Leu
NM_001368143.2:c.516T>G	NP_001355072.1:p.Phe172Leu
NM_001368144.2:c.516T>G	NP_001355073.1:p.Phe172Leu