Canonical Allele Identifier: CA363504514

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007526T>C (hg19) ; chr6:g.32039749T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039749T>C , CM000668.2:g.32039749T>C	GRCh38
NC_000006.11:g.32007526T>C , CM000668.1:g.32007526T>C	GRCh37
NC_000006.10:g.32115505T>C	NCBI36
NG_007941.2:g.6442T>C
NG_008337.2:g.74626A>G
NG_007941.3:g.6445T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.652T>C MANE Select	ENSP00000496625.1:p.Phe218Leu
ENST00000418967.6:c.652T>C	ENSP00000408860.2:p.Phe218Leu
ENST00000435122.3:c.562T>C	ENSP00000415043.2:p.Phe188Leu
ENST00000462278.1:n.341T>C
ENST00000464325.5:n.573T>C
ENST00000466779.5:c.*344T>C	ENSP00000417321.1:n.*344T>C
ENST00000466879.5:n.703T>C
ENST00000479074.5:n.710T>C
ENST00000479730.5:n.768T>C
ENST00000483041.5:n.821T>C
ENST00000486063.5:n.832T>C
NM_000500.7:c.652T>C	NP_000491.4:p.Phe218Leu
NM_001128590.3:c.562T>C	NP_001122062.3:p.Phe188Leu
XM_011514314.1:c.247T>C	XP_011512616.1:p.Phe83Leu
NM_000500.9:c.652T>C MANE Select	NP_000491.4:p.Phe218Leu
NM_001368143.1:c.247T>C	NP_001355072.1:p.Phe83Leu
NM_001368144.1:c.247T>C	NP_001355073.1:p.Phe83Leu
NM_001128590.4:c.562T>C	NP_001122062.3:p.Phe188Leu
NM_001368143.2:c.247T>C	NP_001355072.1:p.Phe83Leu
NM_001368144.2:c.247T>C	NP_001355073.1:p.Phe83Leu