Canonical Allele Identifier: CA363511650
Gene: CYP21A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32040867A>C , CM000668.2:g.32040867A>C GRCh38
NC_000006.11:g.32008644A>C , CM000668.1:g.32008644A>C GRCh37
NC_000006.10:g.32116623A>C NCBI36
NG_007941.2:g.7560A>C
NG_008337.2:g.73508T>G
NG_007941.3:g.7563A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644719.2:c.1223-2A>C MANE Select ENSP00000496625.1:n.1223-2A>C
ENST00000418967.6:c.1223-2A>C ENSP00000408860.2:n.1223-2A>C
ENST00000435122.3:c.1133-2A>C ENSP00000415043.2:n.1133-2A>C
ENST00000479074.5:n.1364-2A>C
ENST00000479730.5:n.1339-2A>C
ENST00000483041.5:n.1392-2A>C
ENST00000486063.5:n.1202-2A>C
NM_000500.7:c.1223-2A>C NP_000491.4:n.1223-2A>C
NM_001128590.3:c.1133-2A>C NP_001122062.3:n.1133-2A>C
XM_011514314.1:c.818-2A>C XP_011512616.1:n.818-2A>C
NM_000500.9:c.1223-2A>C MANE Select NP_000491.4:n.1223-2A>C
NM_001368143.1:c.818-2A>C NP_001355072.1:n.818-2A>C
NM_001368144.1:c.818-2A>C NP_001355073.1:n.818-2A>C
NM_001128590.4:c.1133-2A>C NP_001122062.3:n.1133-2A>C
NM_001368143.2:c.818-2A>C NP_001355072.1:n.818-2A>C
NM_001368144.2:c.818-2A>C NP_001355073.1:n.818-2A>C