Canonical Allele Identifier: CA363504365

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32039648-G-C
• MyVariant Identifiers: chr6:g.32007425G>C (hg19) ; chr6:g.32039648G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039648G>C , CM000668.2:g.32039648G>C	GRCh38
NC_000006.11:g.32007425G>C , CM000668.1:g.32007425G>C	GRCh37
NC_000006.10:g.32115404G>C	NCBI36
NG_007941.2:g.6341G>C
NG_008337.2:g.74727C>G
NG_007941.3:g.6344G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.651+1G>C MANE Select	ENSP00000496625.1:n.651+1G>C
ENST00000418967.6:c.651+1G>C	ENSP00000408860.2:n.651+1G>C
ENST00000435122.3:c.561+1G>C	ENSP00000415043.2:n.561+1G>C
ENST00000462278.1:n.240G>C
ENST00000464325.5:n.572+1G>C
ENST00000466779.5:c.*343+1G>C	ENSP00000417321.1:n.*343+1G>C
ENST00000466879.5:n.702+1G>C
ENST00000479074.5:n.709+1G>C
ENST00000479730.5:n.767+1G>C
ENST00000483041.5:n.820+1G>C
ENST00000486063.5:n.831+1G>C
NM_000500.7:c.651+1G>C	NP_000491.4:n.651+1G>C
NM_001128590.3:c.561+1G>C	NP_001122062.3:n.561+1G>C
XM_011514314.1:c.246+1G>C	XP_011512616.1:n.246+1G>C
NM_000500.9:c.651+1G>C MANE Select	NP_000491.4:n.651+1G>C
NM_001368143.1:c.246+1G>C	NP_001355072.1:n.246+1G>C
NM_001368144.1:c.246+1G>C	NP_001355073.1:n.246+1G>C
NM_001128590.4:c.561+1G>C	NP_001122062.3:n.561+1G>C
NM_001368143.2:c.246+1G>C	NP_001355072.1:n.246+1G>C
NM_001368144.2:c.246+1G>C	NP_001355073.1:n.246+1G>C