Canonical Allele Identifier: CA2678089729

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32040603-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040603G>T , CM000668.2:g.32040603G>T	GRCh38
NC_000006.11:g.32008380G>T , CM000668.1:g.32008380G>T	GRCh37
NC_000006.10:g.32116359G>T	NCBI36
NG_007941.2:g.7296G>T
NG_008337.2:g.73772C>A
NG_007941.3:g.7299G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1118+19G>T MANE Select	ENSP00000496625.1:n.1118+19G>T
ENST00000418967.6:c.1118+19G>T	ENSP00000408860.2:n.1118+19G>T
ENST00000435122.3:c.1028+19G>T	ENSP00000415043.2:n.1028+19G>T
ENST00000479074.5:n.1195G>T
ENST00000479730.5:n.1234+19G>T
ENST00000483041.5:n.1287+19G>T
ENST00000486063.5:n.1097+19G>T
NM_000500.7:c.1118+19G>T	NP_000491.4:n.1118+19G>T
NM_001128590.3:c.1028+19G>T	NP_001122062.3:n.1028+19G>T
XM_011514314.1:c.713+19G>T	XP_011512616.1:n.713+19G>T
NM_000500.9:c.1118+19G>T MANE Select	NP_000491.4:n.1118+19G>T
NM_001368143.1:c.713+19G>T	NP_001355072.1:n.713+19G>T
NM_001368144.1:c.713+19G>T	NP_001355073.1:n.713+19G>T
NM_001128590.4:c.1028+19G>T	NP_001122062.3:n.1028+19G>T
NM_001368143.2:c.713+19G>T	NP_001355072.1:n.713+19G>T
NM_001368144.2:c.713+19G>T	NP_001355073.1:n.713+19G>T