Canonical Allele Identifier: CA363510722

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008228G>C (hg19) ; chr6:g.32040451G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040451G>C , CM000668.2:g.32040451G>C	GRCh38
NC_000006.11:g.32008228G>C , CM000668.1:g.32008228G>C	GRCh37
NC_000006.10:g.32116207G>C	NCBI36
NG_007941.2:g.7144G>C
NG_008337.2:g.73924C>G
NG_007941.3:g.7147G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.985G>C MANE Select	ENSP00000496625.1:p.Gly329Arg
ENST00000418967.6:c.985G>C	ENSP00000408860.2:p.Gly329Arg
ENST00000435122.3:c.895G>C	ENSP00000415043.2:p.Gly299Arg
ENST00000479074.5:n.1043G>C
ENST00000479730.5:n.1101G>C
ENST00000483041.5:n.1154G>C
ENST00000486063.5:n.964G>C
NM_000500.7:c.985G>C	NP_000491.4:p.Gly329Arg
NM_001128590.3:c.895G>C	NP_001122062.3:p.Gly299Arg
XM_011514314.1:c.580G>C	XP_011512616.1:p.Gly194Arg
NM_000500.9:c.985G>C MANE Select	NP_000491.4:p.Gly329Arg
NM_001368143.1:c.580G>C	NP_001355072.1:p.Gly194Arg
NM_001368144.1:c.580G>C	NP_001355073.1:p.Gly194Arg
NM_001128590.4:c.895G>C	NP_001122062.3:p.Gly299Arg
NM_001368143.2:c.580G>C	NP_001355072.1:p.Gly194Arg
NM_001368144.2:c.580G>C	NP_001355073.1:p.Gly194Arg