Canonical Allele Identifier: CA363511771

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008669A>G (hg19) ; chr6:g.32040892A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040892A>G , CM000668.2:g.32040892A>G	GRCh38
NC_000006.11:g.32008669A>G , CM000668.1:g.32008669A>G	GRCh37
NC_000006.10:g.32116648A>G	NCBI36
NG_007941.2:g.7585A>G
NG_008337.2:g.73483T>C
NG_007941.3:g.7588A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1246A>G MANE Select	ENSP00000496625.1:p.Asn416Asp
ENST00000418967.6:c.1246A>G	ENSP00000408860.2:p.Asn416Asp
ENST00000435122.3:c.1156A>G	ENSP00000415043.2:p.Asn386Asp
ENST00000479074.5:n.1387A>G
ENST00000479730.5:n.1362A>G
ENST00000483041.5:n.1415A>G
ENST00000486063.5:n.1225A>G
NM_000500.7:c.1246A>G	NP_000491.4:p.Asn416Asp
NM_001128590.3:c.1156A>G	NP_001122062.3:p.Asn386Asp
XM_011514314.1:c.841A>G	XP_011512616.1:p.Asn281Asp
NM_000500.9:c.1246A>G MANE Select	NP_000491.4:p.Asn416Asp
NM_001368143.1:c.841A>G	NP_001355072.1:p.Asn281Asp
NM_001368144.1:c.841A>G	NP_001355073.1:p.Asn281Asp
NM_001128590.4:c.1156A>G	NP_001122062.3:p.Asn386Asp
NM_001368143.2:c.841A>G	NP_001355072.1:p.Asn281Asp
NM_001368144.2:c.841A>G	NP_001355073.1:p.Asn281Asp