Canonical Allele Identifier: CA1825496366

Gene: CYP11B1 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142875407A= , CM000670.2:g.142875407A=	GRCh38
NC_000008.10:g.143956823A= , CM000670.1:g.143956823A=	GRCh37
NC_000008.9:g.143953825A=	NCBI36
NG_007954.1:g.9414T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.1122-95T= (CYP11B1) MANE Select	ENSP00000292427.5:n.1122-95T=
ENST00000292427.8:c.1122-95T= (CYP11B1)	ENSP00000292427.4:n.1122-95T=
ENST00000314111.4:n.1517-95T= (CYP11B1)
ENST00000377675.3:c.1335-95T= (CYP11B1)	ENSP00000366903.3:n.1335-95T=
ENST00000517471.5:c.1122-95T= (CYP11B1)	ENSP00000428043.1:n.1122-95T=
ENST00000519285.5:c.87-26T= (CYP11B1)	ENSP00000430144.1:n.87-26T=
ENST00000522728.5:c.181+34182A= (GML)	ENSP00000430799.1:n.181+34182A=
NM_000497.3:c.1122-95T= (CYP11B1)	NP_000488.3:n.1122-95T=
NM_001026213.1:c.1122-95T= (CYP11B1)	NP_001021384.1:n.1122-95T=
XM_011516870.1:c.1200-26T= (CYP11B1)	XP_011515172.1:n.1200-26T=
XM_011516871.1:c.1200-95T= (CYP11B1)	XP_011515173.1:n.1200-95T=
XM_011516872.1:c.1122-26T= (CYP11B1)	XP_011515174.1:n.1122-26T=
XM_011516873.1:c.1200-26T= (CYP11B1)	XP_011515175.1:n.1200-26T=
XM_011516874.1:c.1200-95T= (CYP11B1)	XP_011515176.1:n.1200-95T=
XM_011516875.1:c.939-26T= (CYP11B1)	XP_011515177.1:n.939-26T=
XM_011516876.1:c.1200-26T= (CYP11B1)	XP_011515178.1:n.1200-26T=
XM_011516970.1:c.214+34182A= (GML)	XP_011515272.1:n.214+34182A=
NM_000497.4:c.1122-95T= (CYP11B1) MANE Select	NP_000488.3:n.1122-95T=