Canonical Allele Identifier: CA2678090005

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32040834-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040834A>C , CM000668.2:g.32040834A>C	GRCh38
NC_000006.11:g.32008611A>C , CM000668.1:g.32008611A>C	GRCh37
NC_000006.10:g.32116590A>C	NCBI36
NG_007941.2:g.7527A>C
NG_008337.2:g.73541T>G
NG_007941.3:g.7530A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1223-35A>C MANE Select	ENSP00000496625.1:n.1223-35A>C
ENST00000418967.6:c.1223-35A>C	ENSP00000408860.2:n.1223-35A>C
ENST00000435122.3:c.1133-35A>C	ENSP00000415043.2:n.1133-35A>C
ENST00000479074.5:n.1364-35A>C
ENST00000479730.5:n.1339-35A>C
ENST00000483041.5:n.1392-35A>C
ENST00000486063.5:n.1202-35A>C
NM_000500.7:c.1223-35A>C	NP_000491.4:n.1223-35A>C
NM_001128590.3:c.1133-35A>C	NP_001122062.3:n.1133-35A>C
XM_011514314.1:c.818-35A>C	XP_011512616.1:n.818-35A>C
NM_000500.9:c.1223-35A>C MANE Select	NP_000491.4:n.1223-35A>C
NM_001368143.1:c.818-35A>C	NP_001355072.1:n.818-35A>C
NM_001368144.1:c.818-35A>C	NP_001355073.1:n.818-35A>C
NM_001128590.4:c.1133-35A>C	NP_001122062.3:n.1133-35A>C
NM_001368143.2:c.818-35A>C	NP_001355072.1:n.818-35A>C
NM_001368144.2:c.818-35A>C	NP_001355073.1:n.818-35A>C