Canonical Allele Identifier: CA363510691

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008223G>T (hg19) ; chr6:g.32040446G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040446G>T , CM000668.2:g.32040446G>T	GRCh38
NC_000006.11:g.32008223G>T , CM000668.1:g.32008223G>T	GRCh37
NC_000006.10:g.32116202G>T	NCBI36
NG_007941.2:g.7139G>T
NG_008337.2:g.73929C>A
NG_007941.3:g.7142G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.980G>T MANE Select	ENSP00000496625.1:p.Gly327Val
ENST00000418967.6:c.980G>T	ENSP00000408860.2:p.Gly327Val
ENST00000435122.3:c.890G>T	ENSP00000415043.2:p.Gly297Val
ENST00000479074.5:n.1038G>T
ENST00000479730.5:n.1096G>T
ENST00000483041.5:n.1149G>T
ENST00000486063.5:n.959G>T
NM_000500.7:c.980G>T	NP_000491.4:p.Gly327Val
NM_001128590.3:c.890G>T	NP_001122062.3:p.Gly297Val
XM_011514314.1:c.575G>T	XP_011512616.1:p.Gly192Val
NM_000500.9:c.980G>T MANE Select	NP_000491.4:p.Gly327Val
NM_001368143.1:c.575G>T	NP_001355072.1:p.Gly192Val
NM_001368144.1:c.575G>T	NP_001355073.1:p.Gly192Val
NM_001128590.4:c.890G>T	NP_001122062.3:p.Gly297Val
NM_001368143.2:c.575G>T	NP_001355072.1:p.Gly192Val
NM_001368144.2:c.575G>T	NP_001355073.1:p.Gly192Val