Canonical Allele Identifier: CA3732479

Gene: CYP21A2

Linked Data

• dbSNP Id: rs373413129
• ExAC: 6:32007514 T / C
• gnomAD v2: 6-32007514-T-C
• gnomAD v3: 6-32039737-T-C
• gnomAD v4: 6-32039737-T-C
• MyVariant Identifiers: chr6:g.32007514T>C (hg19) ; chr6:g.32039737T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039737T>C , CM000668.2:g.32039737T>C	GRCh38
NC_000006.11:g.32007514T>C , CM000668.1:g.32007514T>C	GRCh37
NC_000006.10:g.32115493T>C	NCBI36
NG_007941.2:g.6430T>C
NG_008337.2:g.74638A>G
NG_007941.3:g.6433T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.652-12T>C MANE Select	ENSP00000496625.1:n.652-12T>C
ENST00000418967.6:c.652-12T>C	ENSP00000408860.2:n.652-12T>C
ENST00000435122.3:c.562-12T>C	ENSP00000415043.2:n.562-12T>C
ENST00000462278.1:n.329T>C
ENST00000464325.5:n.573-12T>C
ENST00000466779.5:c.*344-12T>C	ENSP00000417321.1:n.*344-12T>C
ENST00000466879.5:n.703-12T>C
ENST00000479074.5:n.710-12T>C
ENST00000479730.5:n.768-12T>C
ENST00000483041.5:n.821-12T>C
ENST00000486063.5:n.832-12T>C
NM_000500.7:c.652-12T>C	NP_000491.4:n.652-12T>C
NM_001128590.3:c.562-12T>C	NP_001122062.3:n.562-12T>C
XM_011514314.1:c.247-12T>C	XP_011512616.1:n.247-12T>C
NM_000500.9:c.652-12T>C MANE Select	NP_000491.4:n.652-12T>C
NM_001368143.1:c.247-12T>C	NP_001355072.1:n.247-12T>C
NM_001368144.1:c.247-12T>C	NP_001355073.1:n.247-12T>C
NM_001128590.4:c.562-12T>C	NP_001122062.3:n.562-12T>C
NM_001368143.2:c.247-12T>C	NP_001355072.1:n.247-12T>C
NM_001368144.2:c.247-12T>C	NP_001355073.1:n.247-12T>C