Canonical Allele Identifier: CA363506600

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007854G>C (hg19) ; chr6:g.32040077G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040077G>C , CM000668.2:g.32040077G>C	GRCh38
NC_000006.11:g.32007854G>C , CM000668.1:g.32007854G>C	GRCh37
NC_000006.10:g.32115833G>C	NCBI36
NG_007941.2:g.6770G>C
NG_008337.2:g.74298C>G
NG_007941.3:g.6773G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.811G>C MANE Select	ENSP00000496625.1:p.Glu271Gln
ENST00000418967.6:c.811G>C	ENSP00000408860.2:p.Glu271Gln
ENST00000435122.3:c.721G>C	ENSP00000415043.2:p.Glu241Gln
ENST00000479074.5:n.869G>C
ENST00000479730.5:n.927G>C
ENST00000483041.5:n.980G>C
ENST00000486063.5:n.918+242G>C
NM_000500.7:c.811G>C	NP_000491.4:p.Glu271Gln
NM_001128590.3:c.721G>C	NP_001122062.3:p.Glu241Gln
XM_011514314.1:c.406G>C	XP_011512616.1:p.Glu136Gln
NM_000500.9:c.811G>C MANE Select	NP_000491.4:p.Glu271Gln
NM_001368143.1:c.406G>C	NP_001355072.1:p.Glu136Gln
NM_001368144.1:c.406G>C	NP_001355073.1:p.Glu136Gln
NM_001128590.4:c.721G>C	NP_001122062.3:p.Glu241Gln
NM_001368143.2:c.406G>C	NP_001355072.1:p.Glu136Gln
NM_001368144.2:c.406G>C	NP_001355073.1:p.Glu136Gln