Canonical Allele Identifier: CA363504747

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007547C>G (hg19) ; chr6:g.32039770C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039770C>G , CM000668.2:g.32039770C>G	GRCh38
NC_000006.11:g.32007547C>G , CM000668.1:g.32007547C>G	GRCh37
NC_000006.10:g.32115526C>G	NCBI36
NG_007941.2:g.6463C>G
NG_008337.2:g.74605G>C
NG_007941.3:g.6466C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.673C>G MANE Select	ENSP00000496625.1:p.Arg225Gly
ENST00000418967.6:c.673C>G	ENSP00000408860.2:p.Arg225Gly
ENST00000435122.3:c.583C>G	ENSP00000415043.2:p.Arg195Gly
ENST00000462278.1:n.362C>G
ENST00000466779.5:c.*365C>G	ENSP00000417321.1:n.*365C>G
ENST00000466879.5:n.724C>G
ENST00000479074.5:n.731C>G
ENST00000479730.5:n.789C>G
ENST00000483041.5:n.842C>G
ENST00000486063.5:n.853C>G
NM_000500.7:c.673C>G	NP_000491.4:p.Arg225Gly
NM_001128590.3:c.583C>G	NP_001122062.3:p.Arg195Gly
XM_011514314.1:c.268C>G	XP_011512616.1:p.Arg90Gly
NM_000500.9:c.673C>G MANE Select	NP_000491.4:p.Arg225Gly
NM_001368143.1:c.268C>G	NP_001355072.1:p.Arg90Gly
NM_001368144.1:c.268C>G	NP_001355073.1:p.Arg90Gly
NM_001128590.4:c.583C>G	NP_001122062.3:p.Arg195Gly
NM_001368143.2:c.268C>G	NP_001355072.1:p.Arg90Gly
NM_001368144.2:c.268C>G	NP_001355073.1:p.Arg90Gly