Canonical Allele Identifier: CA363506216

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007826G>T (hg19) ; chr6:g.32040049G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040049G>T , CM000668.2:g.32040049G>T	GRCh38
NC_000006.11:g.32007826G>T , CM000668.1:g.32007826G>T	GRCh37
NC_000006.10:g.32115805G>T	NCBI36
NG_007941.2:g.6742G>T
NG_008337.2:g.74326C>A
NG_007941.3:g.6745G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.783G>T MANE Select	ENSP00000496625.1:p.Met261Ile
ENST00000418967.6:c.783G>T	ENSP00000408860.2:p.Met261Ile
ENST00000435122.3:c.693G>T	ENSP00000415043.2:p.Met231Ile
ENST00000479074.5:n.841G>T
ENST00000479730.5:n.899G>T
ENST00000483041.5:n.952G>T
ENST00000486063.5:n.918+214G>T
NM_000500.7:c.783G>T	NP_000491.4:p.Met261Ile
NM_001128590.3:c.693G>T	NP_001122062.3:p.Met231Ile
XM_011514314.1:c.378G>T	XP_011512616.1:p.Met126Ile
NM_000500.9:c.783G>T MANE Select	NP_000491.4:p.Met261Ile
NM_001368143.1:c.378G>T	NP_001355072.1:p.Met126Ile
NM_001368144.1:c.378G>T	NP_001355073.1:p.Met126Ile
NM_001128590.4:c.693G>T	NP_001122062.3:p.Met231Ile
NM_001368143.2:c.378G>T	NP_001355072.1:p.Met126Ile
NM_001368144.2:c.378G>T	NP_001355073.1:p.Met126Ile