Canonical Allele Identifier: CA1825515736

Gene: CYP11B2 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142914735A= , CM000670.2:g.142914735A=	GRCh38
NC_000008.10:g.143996151A= , CM000670.1:g.143996151A=	GRCh37
NC_000008.9:g.143993153A=	NCBI36
NG_008374.1:g.8109T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323110.2:c.769T= (CYP11B2) MANE Select	ENSP00000325822.2:p.Phe257=
ENST00000522728.5:c.264+690A= (GML)	ENSP00000430799.1:n.264+690A=
NM_000498.3:c.769T= (CYP11B2) MANE Select	NP_000489.3:p.Phe257=
XM_011516877.1:c.847T= (CYP11B2)	XP_011515179.1:p.Phe283=
XM_011516878.1:c.847T= (CYP11B2)	XP_011515180.1:p.Phe283=
XM_011516879.1:c.769T= (CYP11B2)	XP_011515181.1:p.Phe257=
XM_011516970.1:c.297+690A= (GML)	XP_011515272.1:n.297+690A=