Canonical Allele Identifier: CA1825514074

Gene: CYP11B2 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142911839T= , CM000670.2:g.142911839T=	GRCh38
NC_000008.10:g.143993255T= , CM000670.1:g.143993255T=	GRCh37
NC_000008.9:g.143990257T=	NCBI36
NG_008374.1:g.11005A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000323110.2:c.*141A= (CYP11B2) MANE Select	ENSP00000325822.2:n.*141A=
ENST00000522728.5:c.182-2124T= (GML)	ENSP00000430799.1:n.182-2124T=
NM_000498.3:c.*141A= (CYP11B2) MANE Select	NP_000489.3:n.*141A=
XM_011516877.1:c.*141A= (CYP11B2)	XP_011515179.1:n.*141A=
XM_011516878.1:c.*141A= (CYP11B2)	XP_011515180.1:n.*141A=
XM_011516879.1:c.*141A= (CYP11B2)	XP_011515181.1:n.*141A=
XM_011516970.1:c.215-2124T= (GML)	XP_011515272.1:n.215-2124T=