Canonical Allele Identifier: CA449818958

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32040725-C-G
• MyVariant Identifiers: chr6:g.32008502C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040725C>G , CM000668.2:g.32040725C>G	GRCh38
NC_000006.11:g.32008502C>G , CM000668.1:g.32008502C>G	GRCh37
NC_000006.10:g.32116481C>G	NCBI36
NG_007941.2:g.7418C>G
NG_008337.2:g.73650G>C
NG_007941.3:g.7421C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1176C>G MANE Select	ENSP00000496625.1:p.Ala392=
ENST00000418967.6:c.1176C>G	ENSP00000408860.2:p.Ala392=
ENST00000435122.3:c.1086C>G	ENSP00000415043.2:p.Ala362=
ENST00000479074.5:n.1317C>G
ENST00000479730.5:n.1292C>G
ENST00000483041.5:n.1345C>G
ENST00000486063.5:n.1155C>G
NM_000500.7:c.1176C>G	NP_000491.4:p.Ala392=
NM_001128590.3:c.1086C>G	NP_001122062.3:p.Ala362=
XM_011514314.1:c.771C>G	XP_011512616.1:p.Ala257=
NM_000500.9:c.1176C>G MANE Select	NP_000491.4:p.Ala392=
NM_001368143.1:c.771C>G	NP_001355072.1:p.Ala257=
NM_001368144.1:c.771C>G	NP_001355073.1:p.Ala257=
NM_001128590.4:c.1086C>G	NP_001122062.3:p.Ala362=
NM_001368143.2:c.771C>G	NP_001355072.1:p.Ala257=
NM_001368144.2:c.771C>G	NP_001355073.1:p.Ala257=