Canonical Allele Identifier: CA1825515724

Gene: CYP11B2 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142914708A= , CM000670.2:g.142914708A=	GRCh38
NC_000008.10:g.143996124A= , CM000670.1:g.143996124A=	GRCh37
NC_000008.9:g.143993126A=	NCBI36
NG_008374.1:g.8136T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323110.2:c.796T= (CYP11B2) MANE Select	ENSP00000325822.2:p.Tyr266=
ENST00000522728.5:c.264+663A= (GML)	ENSP00000430799.1:n.264+663A=
NM_000498.3:c.796T= (CYP11B2) MANE Select	NP_000489.3:p.Tyr266=
XM_011516877.1:c.874T= (CYP11B2)	XP_011515179.1:p.Tyr292=
XM_011516878.1:c.874T= (CYP11B2)	XP_011515180.1:p.Tyr292=
XM_011516879.1:c.796T= (CYP11B2)	XP_011515181.1:p.Tyr266=
XM_011516970.1:c.297+663A= (GML)	XP_011515272.1:n.297+663A=