Canonical Allele Identifier: CA449818573

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007409G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039632G>T , CM000668.2:g.32039632G>T	GRCh38
NC_000006.11:g.32007409G>T , CM000668.1:g.32007409G>T	GRCh37
NC_000006.10:g.32115388G>T	NCBI36
NG_007941.2:g.6325G>T
NG_008337.2:g.74743C>A
NG_007941.3:g.6328G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.636G>T MANE Select	ENSP00000496625.1:p.Val212=
ENST00000418967.6:c.636G>T	ENSP00000408860.2:p.Val212=
ENST00000435122.3:c.546G>T	ENSP00000415043.2:p.Val182=
ENST00000462278.1:n.224G>T
ENST00000464325.5:n.557G>T
ENST00000466779.5:c.*328G>T	ENSP00000417321.1:n.*328G>T
ENST00000466879.5:n.687G>T
ENST00000469053.5:c.*328G>T	ENSP00000418104.1:n.*328G>T
ENST00000479074.5:n.694G>T
ENST00000479730.5:n.752G>T
ENST00000483041.5:n.805G>T
ENST00000486063.5:n.816G>T
NM_000500.7:c.636G>T	NP_000491.4:p.Val212=
NM_001128590.3:c.546G>T	NP_001122062.3:p.Val182=
XM_011514314.1:c.231G>T	XP_011512616.1:p.Val77=
NM_000500.9:c.636G>T MANE Select	NP_000491.4:p.Val212=
NM_001368143.1:c.231G>T	NP_001355072.1:p.Val77=
NM_001368144.1:c.231G>T	NP_001355073.1:p.Val77=
NM_001128590.4:c.546G>T	NP_001122062.3:p.Val182=
NM_001368143.2:c.231G>T	NP_001355072.1:p.Val77=
NM_001368144.2:c.231G>T	NP_001355073.1:p.Val77=