Canonical Allele Identifier: CA2578617952

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038352A>T , CM000668.2:g.32038352A>T	GRCh38
NC_000006.11:g.32006129A>T , CM000668.1:g.32006129A>T	GRCh37
NC_000006.10:g.32114108A>T	NCBI36
NG_007941.2:g.5048A>T
NG_007941.3:g.5048A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418967.6:c.-71A>T	ENSP00000408860.2:n.-71A>T
ENST00000466779.5:c.-71A>T	ENSP00000417321.1:n.-71A>T
ENST00000486063.5:n.13A>T
NM_000500.7:c.-71A>T	NP_000491.4:n.-71A>T
NM_001128590.3:c.-71A>T	NP_001122062.3:n.-71A>T
NM_001368143.1:c.-495A>T	NP_001355072.1:n.-495A>T
NM_001368144.1:c.-405A>T	NP_001355073.1:n.-405A>T