Canonical Allele Identifier: CA3732562
Gene: CYP21A2 HGNC NCBI

Linked Data

dbSNP Id: rs753678267
gnomAD v2: 6-32007928-G-A
gnomAD v3: 6-32040151-G-A
gnomAD v4: 6-32040151-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32040151G>A , CM000668.2:g.32040151G>A GRCh38
NC_000006.11:g.32007928G>A , CM000668.1:g.32007928G>A GRCh37
NC_000006.10:g.32115907G>A NCBI36
NG_007941.2:g.6844G>A
NG_008337.2:g.74224C>T
NG_007941.3:g.6847G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.885G>A MANE Select ENSP00000496625.1:p.Glu295=
ENST00000418967.6:c.885G>A ENSP00000408860.2:p.Glu295=
ENST00000435122.3:c.795G>A ENSP00000415043.2:p.Glu265=
ENST00000479074.5:n.943G>A
ENST00000479730.5:n.1001G>A
ENST00000483041.5:n.1054G>A
ENST00000486063.5:n.919-255G>A
NM_000500.7:c.885G>A NP_000491.4:p.Glu295=
NM_001128590.3:c.795G>A NP_001122062.3:p.Glu265=
XM_011514314.1:c.480G>A XP_011512616.1:p.Glu160=
NM_000500.9:c.885G>A MANE Select NP_000491.4:p.Glu295=
NM_001368143.1:c.480G>A NP_001355072.1:p.Glu160=
NM_001368144.1:c.480G>A NP_001355073.1:p.Glu160=
NM_001128590.4:c.795G>A NP_001122062.3:p.Glu265=
NM_001368143.2:c.480G>A NP_001355072.1:p.Glu160=
NM_001368144.2:c.480G>A NP_001355073.1:p.Glu160=