Canonical Allele Identifier: CA1825497234

Gene: CYP11B1 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142876776G= , CM000670.2:g.142876776G=	GRCh38
NC_000008.10:g.143958192G= , CM000670.1:g.143958192G=	GRCh37
NC_000008.9:g.143955194G=	NCBI36
NG_007954.1:g.8045C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.705C= (CYP11B1) MANE Select	ENSP00000292427.5:p.Val235=
ENST00000292427.8:c.705C= (CYP11B1)	ENSP00000292427.4:p.Val235=
ENST00000314111.4:n.738C= (CYP11B1)
ENST00000377675.3:c.918C= (CYP11B1)	ENSP00000366903.3:p.Val306=
ENST00000517471.5:c.705C= (CYP11B1)	ENSP00000428043.1:p.Val235=
ENST00000522728.5:c.181+35551G= (GML)	ENSP00000430799.1:n.181+35551G=
NM_000497.3:c.705C= (CYP11B1)	NP_000488.3:p.Val235=
NM_001026213.1:c.705C= (CYP11B1)	NP_001021384.1:p.Val235=
XM_011516870.1:c.783C= (CYP11B1)	XP_011515172.1:p.Val261=
XM_011516871.1:c.783C= (CYP11B1)	XP_011515173.1:p.Val261=
XM_011516872.1:c.705C= (CYP11B1)	XP_011515174.1:p.Val235=
XM_011516873.1:c.783C= (CYP11B1)	XP_011515175.1:p.Val261=
XM_011516874.1:c.783C= (CYP11B1)	XP_011515176.1:p.Val261=
XM_011516875.1:c.522C= (CYP11B1)	XP_011515177.1:p.Val174=
XM_011516876.1:c.783C= (CYP11B1)	XP_011515178.1:p.Val261=
XM_011516970.1:c.214+35551G= (GML)	XP_011515272.1:n.214+35551G=
NM_000497.4:c.705C= (CYP11B1) MANE Select	NP_000488.3:p.Val235=