Canonical Allele Identifier: CA363512768

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008906C>T (hg19) ; chr6:g.32041129C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32041129C>T , CM000668.2:g.32041129C>T	GRCh38
NC_000006.11:g.32008906C>T , CM000668.1:g.32008906C>T	GRCh37
NC_000006.10:g.32116885C>T	NCBI36
NG_007941.2:g.7822C>T
NG_008337.2:g.73246G>A
NG_007941.3:g.7825C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1483C>T MANE Select	ENSP00000496625.1:p.Gln495Ter
ENST00000418967.6:c.1483C>T	ENSP00000408860.2:p.Gln495Ter
ENST00000435122.3:c.1393C>T	ENSP00000415043.2:p.Gln465Ter
ENST00000479074.5:n.1624C>T
ENST00000479730.5:n.1599C>T
ENST00000483041.5:n.1652C>T
ENST00000486063.5:n.1462C>T
NM_000500.7:c.1483C>T	NP_000491.4:p.Gln495Ter
NM_001128590.3:c.1393C>T	NP_001122062.3:p.Gln465Ter
XM_011514314.1:c.1078C>T	XP_011512616.1:p.Gln360Ter
NM_000500.9:c.1483C>T MANE Select	NP_000491.4:p.Gln495Ter
NM_001368143.1:c.1078C>T	NP_001355072.1:p.Gln360Ter
NM_001368144.1:c.1078C>T	NP_001355073.1:p.Gln360Ter
NM_001128590.4:c.1393C>T	NP_001122062.3:p.Gln465Ter
NM_001368143.2:c.1078C>T	NP_001355072.1:p.Gln360Ter
NM_001368144.2:c.1078C>T	NP_001355073.1:p.Gln360Ter