Canonical Allele Identifier: CA566693922

Gene: CYP21A2

Linked Data

• dbSNP Id: rs6459
• gnomAD v2: 6-32007625-C-G
• gnomAD v4: 6-32039848-C-G
• MyVariant Identifiers: chr6:g.32007625C>G (hg19) ; chr6:g.32039848C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039848C>G , CM000668.2:g.32039848C>G	GRCh38
NC_000006.11:g.32007625C>G , CM000668.1:g.32007625C>G	GRCh37
NC_000006.10:g.32115604C>G	NCBI36
NG_007941.2:g.6541C>G
NG_008337.2:g.74527G>C
NG_007941.3:g.6544C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.738+13C>G MANE Select	ENSP00000496625.1:n.738+13C>G
ENST00000418967.6:c.738+13C>G	ENSP00000408860.2:n.738+13C>G
ENST00000435122.3:c.648+13C>G	ENSP00000415043.2:n.648+13C>G
ENST00000462278.1:n.440C>G
ENST00000479074.5:n.796+13C>G
ENST00000479730.5:n.854+13C>G
ENST00000483041.5:n.907+13C>G
ENST00000486063.5:n.918+13C>G
NM_000500.7:c.738+13C>G	NP_000491.4:n.738+13C>G
NM_001128590.3:c.648+13C>G	NP_001122062.3:n.648+13C>G
XM_011514314.1:c.333+13C>G	XP_011512616.1:n.333+13C>G
NM_000500.9:c.738+13C>G MANE Select	NP_000491.4:n.738+13C>G
NM_001368143.1:c.333+13C>G	NP_001355072.1:n.333+13C>G
NM_001368144.1:c.333+13C>G	NP_001355073.1:n.333+13C>G
NM_001128590.4:c.648+13C>G	NP_001122062.3:n.648+13C>G
NM_001368143.2:c.333+13C>G	NP_001355072.1:n.333+13C>G
NM_001368144.2:c.333+13C>G	NP_001355073.1:n.333+13C>G