Canonical Allele Identifier: CA363506153

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1776174302
• MyVariant Identifiers: chr6:g.32007822A>G (hg19) ; chr6:g.32040045A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040045A>G , CM000668.2:g.32040045A>G	GRCh38
NC_000006.11:g.32007822A>G , CM000668.1:g.32007822A>G	GRCh37
NC_000006.10:g.32115801A>G	NCBI36
NG_007941.2:g.6738A>G
NG_008337.2:g.74330T>C
NG_007941.3:g.6741A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.779A>G MANE Select	ENSP00000496625.1:p.Tyr260Cys
ENST00000418967.6:c.779A>G	ENSP00000408860.2:p.Tyr260Cys
ENST00000435122.3:c.689A>G	ENSP00000415043.2:p.Tyr230Cys
ENST00000479074.5:n.837A>G
ENST00000479730.5:n.895A>G
ENST00000483041.5:n.948A>G
ENST00000486063.5:n.918+210A>G
NM_000500.7:c.779A>G	NP_000491.4:p.Tyr260Cys
NM_001128590.3:c.689A>G	NP_001122062.3:p.Tyr230Cys
XM_011514314.1:c.374A>G	XP_011512616.1:p.Tyr125Cys
NM_000500.9:c.779A>G MANE Select	NP_000491.4:p.Tyr260Cys
NM_001368143.1:c.374A>G	NP_001355072.1:p.Tyr125Cys
NM_001368144.1:c.374A>G	NP_001355073.1:p.Tyr125Cys
NM_001128590.4:c.689A>G	NP_001122062.3:p.Tyr230Cys
NM_001368143.2:c.374A>G	NP_001355072.1:p.Tyr125Cys
NM_001368144.2:c.374A>G	NP_001355073.1:p.Tyr125Cys