Canonical Allele Identifier: CA449818584

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007422A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039645A>C , CM000668.2:g.32039645A>C	GRCh38
NC_000006.11:g.32007422A>C , CM000668.1:g.32007422A>C	GRCh37
NC_000006.10:g.32115401A>C	NCBI36
NG_007941.2:g.6338A>C
NG_008337.2:g.74730T>G
NG_007941.3:g.6341A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.649A>C MANE Select	ENSP00000496625.1:p.Arg217=
ENST00000418967.6:c.649A>C	ENSP00000408860.2:p.Arg217=
ENST00000435122.3:c.559A>C	ENSP00000415043.2:p.Arg187=
ENST00000462278.1:n.237A>C
ENST00000464325.5:n.570A>C
ENST00000466779.5:c.*341A>C	ENSP00000417321.1:n.*341A>C
ENST00000466879.5:n.700A>C
ENST00000479074.5:n.707A>C
ENST00000479730.5:n.765A>C
ENST00000483041.5:n.818A>C
ENST00000486063.5:n.829A>C
NM_000500.7:c.649A>C	NP_000491.4:p.Arg217=
NM_001128590.3:c.559A>C	NP_001122062.3:p.Arg187=
XM_011514314.1:c.244A>C	XP_011512616.1:p.Arg82=
NM_000500.9:c.649A>C MANE Select	NP_000491.4:p.Arg217=
NM_001368143.1:c.244A>C	NP_001355072.1:p.Arg82=
NM_001368144.1:c.244A>C	NP_001355073.1:p.Arg82=
NM_001128590.4:c.559A>C	NP_001122062.3:p.Arg187=
NM_001368143.2:c.244A>C	NP_001355072.1:p.Arg82=
NM_001368144.2:c.244A>C	NP_001355073.1:p.Arg82=