Canonical Allele Identifier: CA2678088587

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32039719-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039719A>C , CM000668.2:g.32039719A>C	GRCh38
NC_000006.11:g.32007496A>C , CM000668.1:g.32007496A>C	GRCh37
NC_000006.10:g.32115475A>C	NCBI36
NG_007941.2:g.6412A>C
NG_008337.2:g.74656T>G
NG_007941.3:g.6415A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.652-30A>C MANE Select	ENSP00000496625.1:n.652-30A>C
ENST00000418967.6:c.652-30A>C	ENSP00000408860.2:n.652-30A>C
ENST00000435122.3:c.562-30A>C	ENSP00000415043.2:n.562-30A>C
ENST00000462278.1:n.311A>C
ENST00000464325.5:n.573-30A>C
ENST00000466779.5:c.*344-30A>C	ENSP00000417321.1:n.*344-30A>C
ENST00000466879.5:n.703-30A>C
ENST00000479074.5:n.710-30A>C
ENST00000479730.5:n.768-30A>C
ENST00000483041.5:n.821-30A>C
ENST00000486063.5:n.832-30A>C
NM_000500.7:c.652-30A>C	NP_000491.4:n.652-30A>C
NM_001128590.3:c.562-30A>C	NP_001122062.3:n.562-30A>C
XM_011514314.1:c.247-30A>C	XP_011512616.1:n.247-30A>C
NM_000500.9:c.652-30A>C MANE Select	NP_000491.4:n.652-30A>C
NM_001368143.1:c.247-30A>C	NP_001355072.1:n.247-30A>C
NM_001368144.1:c.247-30A>C	NP_001355073.1:n.247-30A>C
NM_001128590.4:c.562-30A>C	NP_001122062.3:n.562-30A>C
NM_001368143.2:c.247-30A>C	NP_001355072.1:n.247-30A>C
NM_001368144.2:c.247-30A>C	NP_001355073.1:n.247-30A>C