Canonical Allele Identifier: CA449819016

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008758A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040981A>C , CM000668.2:g.32040981A>C	GRCh38
NC_000006.11:g.32008758A>C , CM000668.1:g.32008758A>C	GRCh37
NC_000006.10:g.32116737A>C	NCBI36
NG_007941.2:g.7674A>C
NG_008337.2:g.73394T>G
NG_007941.3:g.7677A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1335A>C MANE Select	ENSP00000496625.1:p.Arg445=
ENST00000418967.6:c.1335A>C	ENSP00000408860.2:p.Arg445=
ENST00000435122.3:c.1245A>C	ENSP00000415043.2:p.Arg415=
ENST00000479074.5:n.1476A>C
ENST00000479730.5:n.1451A>C
ENST00000483041.5:n.1504A>C
ENST00000486063.5:n.1314A>C
NM_000500.7:c.1335A>C	NP_000491.4:p.Arg445=
NM_001128590.3:c.1245A>C	NP_001122062.3:p.Arg415=
XM_011514314.1:c.930A>C	XP_011512616.1:p.Arg310=
NM_000500.9:c.1335A>C MANE Select	NP_000491.4:p.Arg445=
NM_001368143.1:c.930A>C	NP_001355072.1:p.Arg310=
NM_001368144.1:c.930A>C	NP_001355073.1:p.Arg310=
NM_001128590.4:c.1245A>C	NP_001122062.3:p.Arg415=
NM_001368143.2:c.930A>C	NP_001355072.1:p.Arg310=
NM_001368144.2:c.930A>C	NP_001355073.1:p.Arg310=