Canonical Allele Identifier: CA1619396307
Gene: CYP21A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32038357G= , CM000668.2:g.32038357G= GRCh38
NC_000006.11:g.32006134G= , CM000668.1:g.32006134G= GRCh37
NC_000006.10:g.32114113G= NCBI36
NG_007941.2:g.5053G=
NG_007941.3:g.5053G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000418967.6:c.-66G= ENSP00000408860.2:n.-66G=
ENST00000466779.5:c.-66G= ENSP00000417321.1:n.-66G=
ENST00000486063.5:n.18G=
NM_000500.7:c.-66G= NP_000491.4:n.-66G=
NM_001128590.3:c.-66G= NP_001122062.3:n.-66G=
NM_001368143.1:c.-490G= NP_001355072.1:n.-490G=
NM_001368144.1:c.-400G= NP_001355073.1:n.-400G=