Canonical Allele Identifier: CA1825496996

Gene: CYP11B1 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142876394G= , CM000670.2:g.142876394G=	GRCh38
NC_000008.10:g.143957810G= , CM000670.1:g.143957810G=	GRCh37
NC_000008.9:g.143954812G=	NCBI36
NG_007954.1:g.8427C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.801C= (CYP11B1) MANE Select	ENSP00000292427.5:p.Gly267=
ENST00000292427.8:c.801C= (CYP11B1)	ENSP00000292427.4:p.Gly267=
ENST00000314111.4:n.834C= (CYP11B1)
ENST00000377675.3:c.1014C= (CYP11B1)	ENSP00000366903.3:p.Gly338=
ENST00000517471.5:c.801C= (CYP11B1)	ENSP00000428043.1:p.Gly267=
ENST00000522728.5:c.181+35169G= (GML)	ENSP00000430799.1:n.181+35169G=
NM_000497.3:c.801C= (CYP11B1)	NP_000488.3:p.Gly267=
NM_001026213.1:c.801C= (CYP11B1)	NP_001021384.1:p.Gly267=
XM_011516870.1:c.879C= (CYP11B1)	XP_011515172.1:p.Gly293=
XM_011516871.1:c.879C= (CYP11B1)	XP_011515173.1:p.Gly293=
XM_011516872.1:c.801C= (CYP11B1)	XP_011515174.1:p.Gly267=
XM_011516873.1:c.879C= (CYP11B1)	XP_011515175.1:p.Gly293=
XM_011516874.1:c.879C= (CYP11B1)	XP_011515176.1:p.Gly293=
XM_011516875.1:c.618C= (CYP11B1)	XP_011515177.1:p.Gly206=
XM_011516876.1:c.879C= (CYP11B1)	XP_011515178.1:p.Gly293=
XM_011516970.1:c.214+35169G= (GML)	XP_011515272.1:n.214+35169G=
NM_000497.4:c.801C= (CYP11B1) MANE Select	NP_000488.3:p.Gly267=