Canonical Allele Identifier: CA363511371

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008519T>C (hg19) ; chr6:g.32040742T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040742T>C , CM000668.2:g.32040742T>C	GRCh38
NC_000006.11:g.32008519T>C , CM000668.1:g.32008519T>C	GRCh37
NC_000006.10:g.32116498T>C	NCBI36
NG_007941.2:g.7435T>C
NG_008337.2:g.73633A>G
NG_007941.3:g.7438T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1193T>C MANE Select	ENSP00000496625.1:p.Val398Ala
ENST00000418967.6:c.1193T>C	ENSP00000408860.2:p.Val398Ala
ENST00000435122.3:c.1103T>C	ENSP00000415043.2:p.Val368Ala
ENST00000479074.5:n.1334T>C
ENST00000479730.5:n.1309T>C
ENST00000483041.5:n.1362T>C
ENST00000486063.5:n.1172T>C
NM_000500.7:c.1193T>C	NP_000491.4:p.Val398Ala
NM_001128590.3:c.1103T>C	NP_001122062.3:p.Val368Ala
XM_011514314.1:c.788T>C	XP_011512616.1:p.Val263Ala
NM_000500.9:c.1193T>C MANE Select	NP_000491.4:p.Val398Ala
NM_001368143.1:c.788T>C	NP_001355072.1:p.Val263Ala
NM_001368144.1:c.788T>C	NP_001355073.1:p.Val263Ala
NM_001128590.4:c.1103T>C	NP_001122062.3:p.Val368Ala
NM_001368143.2:c.788T>C	NP_001355072.1:p.Val263Ala
NM_001368144.2:c.788T>C	NP_001355073.1:p.Val263Ala