Canonical Allele Identifier: CA566693809

Gene: CYP21A2

Linked Data

• dbSNP Id: rs528002451
• gnomAD v2: 6-32006185-G-A
• MyVariant Identifiers: chr6:g.32006185G>A (hg19) ; chr6:g.32038408G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038408G>A , CM000668.2:g.32038408G>A	GRCh38
NC_000006.11:g.32006185G>A , CM000668.1:g.32006185G>A	GRCh37
NC_000006.10:g.32114164G>A	NCBI36
NG_007941.2:g.5104G>A
NG_007941.3:g.5104G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418967.6:c.-15G>A	ENSP00000408860.2:n.-15G>A
ENST00000466779.5:c.-15G>A	ENSP00000417321.1:n.-15G>A
ENST00000478281.5:c.-15G>A	ENSP00000419572.1:n.-15G>A
ENST00000479074.5:n.44G>A
ENST00000479730.5:n.44G>A
ENST00000480027.1:n.39G>A
ENST00000483041.5:n.39G>A
ENST00000486063.5:n.69G>A
NM_000500.7:c.-15G>A	NP_000491.4:n.-15G>A
NM_001128590.3:c.-15G>A	NP_001122062.3:n.-15G>A
XM_011514314.1:c.-439G>A	XP_011512616.1:n.-439G>A
NM_001368143.1:c.-439G>A	NP_001355072.1:n.-439G>A
NM_001368144.1:c.-349G>A	NP_001355073.1:n.-349G>A