Canonical Allele Identifier: CA3732567
Gene: CYP21A2 HGNC NCBI

Linked Data

dbSNP Id: rs777168794
gnomAD v2: 6-32007952-G-A
gnomAD v3: 6-32040175-G-A
gnomAD v4: 6-32040175-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32040175G>A , CM000668.2:g.32040175G>A GRCh38
NC_000006.11:g.32007952G>A , CM000668.1:g.32007952G>A GRCh37
NC_000006.10:g.32115931G>A NCBI36
NG_007941.2:g.6868G>A
NG_008337.2:g.74200C>T
NG_007941.3:g.6871G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644719.2:c.909G>A MANE Select ENSP00000496625.1:p.Trp303Ter
ENST00000418967.6:c.909G>A ENSP00000408860.2:p.Trp303Ter
ENST00000435122.3:c.819G>A ENSP00000415043.2:p.Trp273Ter
ENST00000479074.5:n.967G>A
ENST00000479730.5:n.1025G>A
ENST00000483041.5:n.1078G>A
ENST00000486063.5:n.919-231G>A
NM_000500.7:c.909G>A NP_000491.4:p.Trp303Ter
NM_001128590.3:c.819G>A NP_001122062.3:p.Trp273Ter
XM_011514314.1:c.504G>A XP_011512616.1:p.Trp168Ter
NM_000500.9:c.909G>A MANE Select NP_000491.4:p.Trp303Ter
NM_001368143.1:c.504G>A NP_001355072.1:p.Trp168Ter
NM_001368144.1:c.504G>A NP_001355073.1:p.Trp168Ter
NM_001128590.4:c.819G>A NP_001122062.3:p.Trp273Ter
NM_001368143.2:c.504G>A NP_001355072.1:p.Trp168Ter
NM_001368144.2:c.504G>A NP_001355073.1:p.Trp168Ter