Canonical Allele Identifier: CA363504721

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1438515396
• gnomAD v2: 6-32007544-C-T
• MyVariant Identifiers: chr6:g.32007544C>T (hg19) ; chr6:g.32039767C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039767C>T , CM000668.2:g.32039767C>T	GRCh38
NC_000006.11:g.32007544C>T , CM000668.1:g.32007544C>T	GRCh37
NC_000006.10:g.32115523C>T	NCBI36
NG_007941.2:g.6460C>T
NG_008337.2:g.74608G>A
NG_007941.3:g.6463C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.670C>T MANE Select	ENSP00000496625.1:p.Leu224Phe
ENST00000418967.6:c.670C>T	ENSP00000408860.2:p.Leu224Phe
ENST00000435122.3:c.580C>T	ENSP00000415043.2:p.Leu194Phe
ENST00000462278.1:n.359C>T
ENST00000466779.5:c.*362C>T	ENSP00000417321.1:n.*362C>T
ENST00000466879.5:n.721C>T
ENST00000479074.5:n.728C>T
ENST00000479730.5:n.786C>T
ENST00000483041.5:n.839C>T
ENST00000486063.5:n.850C>T
NM_000500.7:c.670C>T	NP_000491.4:p.Leu224Phe
NM_001128590.3:c.580C>T	NP_001122062.3:p.Leu194Phe
XM_011514314.1:c.265C>T	XP_011512616.1:p.Leu89Phe
NM_000500.9:c.670C>T MANE Select	NP_000491.4:p.Leu224Phe
NM_001368143.1:c.265C>T	NP_001355072.1:p.Leu89Phe
NM_001368144.1:c.265C>T	NP_001355073.1:p.Leu89Phe
NM_001128590.4:c.580C>T	NP_001122062.3:p.Leu194Phe
NM_001368143.2:c.265C>T	NP_001355072.1:p.Leu89Phe
NM_001368144.2:c.265C>T	NP_001355073.1:p.Leu89Phe