Canonical Allele Identifier: CA363512682

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32041082-T-C
• MyVariant Identifiers: chr6:g.32008859T>C (hg19) ; chr6:g.32041082T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32041082T>C , CM000668.2:g.32041082T>C	GRCh38
NC_000006.11:g.32008859T>C , CM000668.1:g.32008859T>C	GRCh37
NC_000006.10:g.32116838T>C	NCBI36
NG_007941.2:g.7775T>C
NG_008337.2:g.73293A>G
NG_007941.3:g.7778T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1436T>C MANE Select	ENSP00000496625.1:p.Val479Ala
ENST00000418967.6:c.1436T>C	ENSP00000408860.2:p.Val479Ala
ENST00000435122.3:c.1346T>C	ENSP00000415043.2:p.Val449Ala
ENST00000479074.5:n.1577T>C
ENST00000479730.5:n.1552T>C
ENST00000483041.5:n.1605T>C
ENST00000486063.5:n.1415T>C
NM_000500.7:c.1436T>C	NP_000491.4:p.Val479Ala
NM_001128590.3:c.1346T>C	NP_001122062.3:p.Val449Ala
XM_011514314.1:c.1031T>C	XP_011512616.1:p.Val344Ala
NM_000500.9:c.1436T>C MANE Select	NP_000491.4:p.Val479Ala
NM_001368143.1:c.1031T>C	NP_001355072.1:p.Val344Ala
NM_001368144.1:c.1031T>C	NP_001355073.1:p.Val344Ala
NM_001128590.4:c.1346T>C	NP_001122062.3:p.Val449Ala
NM_001368143.2:c.1031T>C	NP_001355072.1:p.Val344Ala
NM_001368144.2:c.1031T>C	NP_001355073.1:p.Val344Ala