Canonical Allele Identifier: CA449729882

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007965T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040188T>C , CM000668.2:g.32040188T>C	GRCh38
NC_000006.11:g.32007965T>C , CM000668.1:g.32007965T>C	GRCh37
NC_000006.10:g.32115944T>C	NCBI36
NG_007941.2:g.6881T>C
NG_008337.2:g.74187A>G
NG_007941.3:g.6884T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.922T>C MANE Select	ENSP00000496625.1:p.Leu308=
ENST00000418967.6:c.922T>C	ENSP00000408860.2:p.Leu308=
ENST00000435122.3:c.832T>C	ENSP00000415043.2:p.Leu278=
ENST00000479074.5:n.980T>C
ENST00000479730.5:n.1038T>C
ENST00000483041.5:n.1091T>C
ENST00000486063.5:n.919-218T>C
NM_000500.7:c.922T>C	NP_000491.4:p.Leu308=
NM_001128590.3:c.832T>C	NP_001122062.3:p.Leu278=
XM_011514314.1:c.517T>C	XP_011512616.1:p.Leu173=
NM_000500.9:c.922T>C MANE Select	NP_000491.4:p.Leu308=
NM_001368143.1:c.517T>C	NP_001355072.1:p.Leu173=
NM_001368144.1:c.517T>C	NP_001355073.1:p.Leu173=
NM_001128590.4:c.832T>C	NP_001122062.3:p.Leu278=
NM_001368143.2:c.517T>C	NP_001355072.1:p.Leu173=
NM_001368144.2:c.517T>C	NP_001355073.1:p.Leu173=