Canonical Allele Identifier: CA823930774

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1178649710
• MyVariant Identifiers: chr6:g.32007446A>G (hg19) ; chr6:g.32039669A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039669A>G , CM000668.2:g.32039669A>G	GRCh38
NC_000006.11:g.32007446A>G , CM000668.1:g.32007446A>G	GRCh37
NC_000006.10:g.32115425A>G	NCBI36
NG_007941.2:g.6362A>G
NG_008337.2:g.74706T>C
NG_007941.3:g.6365A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.651+22A>G MANE Select	ENSP00000496625.1:n.651+22A>G
ENST00000418967.6:c.651+22A>G	ENSP00000408860.2:n.651+22A>G
ENST00000435122.3:c.561+22A>G	ENSP00000415043.2:n.561+22A>G
ENST00000462278.1:n.261A>G
ENST00000464325.5:n.572+22A>G
ENST00000466779.5:c.*343+22A>G	ENSP00000417321.1:n.*343+22A>G
ENST00000466879.5:n.702+22A>G
ENST00000479074.5:n.709+22A>G
ENST00000479730.5:n.767+22A>G
ENST00000483041.5:n.820+22A>G
ENST00000486063.5:n.831+22A>G
NM_000500.7:c.651+22A>G	NP_000491.4:n.651+22A>G
NM_001128590.3:c.561+22A>G	NP_001122062.3:n.561+22A>G
XM_011514314.1:c.246+22A>G	XP_011512616.1:n.246+22A>G
NM_000500.9:c.651+22A>G MANE Select	NP_000491.4:n.651+22A>G
NM_001368143.1:c.246+22A>G	NP_001355072.1:n.246+22A>G
NM_001368144.1:c.246+22A>G	NP_001355073.1:n.246+22A>G
NM_001128590.4:c.561+22A>G	NP_001122062.3:n.561+22A>G
NM_001368143.2:c.246+22A>G	NP_001355072.1:n.246+22A>G
NM_001368144.2:c.246+22A>G	NP_001355073.1:n.246+22A>G