Canonical Allele Identifier: CA1825514476

Gene: CYP11B2 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142912566G= , CM000670.2:g.142912566G=	GRCh38
NC_000008.10:g.143993982G= , CM000670.1:g.143993982G=	GRCh37
NC_000008.9:g.143990984G=	NCBI36
NG_008374.1:g.10278C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323110.2:c.1362C= (CYP11B2) MANE Select	ENSP00000325822.2:p.Arg454=
ENST00000522728.5:c.182-1397G= (GML)	ENSP00000430799.1:n.182-1397G=
NM_000498.3:c.1362C= (CYP11B2) MANE Select	NP_000489.3:p.Arg454=
XM_011516877.1:c.1509C= (CYP11B2)	XP_011515179.1:p.Arg503=
XM_011516878.1:c.1440C= (CYP11B2)	XP_011515180.1:p.Arg480=
XM_011516879.1:c.1431C= (CYP11B2)	XP_011515181.1:p.Arg477=
XM_011516970.1:c.215-1397G= (GML)	XP_011515272.1:n.215-1397G=