Canonical Allele Identifier: CA823931912

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1456084089
• gnomAD v3: 6-32040837-GCCT-G
• gnomAD v4: 6-32040837-GCCT-G
• MyVariant Identifiers: chr6:g.32008615_32008617del (hg19) ; chr6:g.32040838_32040840del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040840_32040842del , CM000668.2:g.32040840_32040842del	GRCh38
NC_000006.11:g.32008617_32008619del , CM000668.1:g.32008617_32008619del	GRCh37
NC_000006.10:g.32116596_32116598del	NCBI36
NG_007941.2:g.7533_7535del
NG_008337.2:g.73535_73537del
NG_007941.3:g.7536_7538del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1223-29_1223-27del MANE Select	ENSP00000496625.1:n.1223-29_1223-27del
ENST00000418967.6:c.1223-29_1223-27del	ENSP00000408860.2:n.1223-29_1223-27del
ENST00000435122.3:c.1133-29_1133-27del	ENSP00000415043.2:n.1133-29_1133-27del
ENST00000479074.5:n.1364-29_1364-27del
ENST00000479730.5:n.1339-29_1339-27del
ENST00000483041.5:n.1392-29_1392-27del
ENST00000486063.5:n.1202-29_1202-27del
NM_000500.7:c.1223-29_1223-27del	NP_000491.4:n.1223-29_1223-27del
NM_001128590.3:c.1133-29_1133-27del	NP_001122062.3:n.1133-29_1133-27del
XM_011514314.1:c.818-29_818-27del	XP_011512616.1:n.818-29_818-27del
NM_000500.9:c.1223-29_1223-27del MANE Select	NP_000491.4:n.1223-29_1223-27del
NM_001368143.1:c.818-29_818-27del	NP_001355072.1:n.818-29_818-27del
NM_001368144.1:c.818-29_818-27del	NP_001355073.1:n.818-29_818-27del
NM_001128590.4:c.1133-29_1133-27del	NP_001122062.3:n.1133-29_1133-27del
NM_001368143.2:c.818-29_818-27del	NP_001355072.1:n.818-29_818-27del
NM_001368144.2:c.818-29_818-27del	NP_001355073.1:n.818-29_818-27del