Canonical Allele Identifier: CA4904946

Gene: CYP11B1 GML

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142874420A>G , CM000670.2:g.142874420A>G	GRCh38
NC_000008.10:g.143955836A>G , CM000670.1:g.143955836A>G	GRCh37
NC_000008.9:g.143952838A>G	NCBI36
NG_007954.1:g.10401T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000497.4:c.1465T>C (CYP11B1) MANE Select	NP_000488.3:p.Leu489=
ENST00000292427.10:c.1465T>C (CYP11B1) MANE Select	ENSP00000292427.5:p.Leu489=
NM_000497.3:c.1465T>C (CYP11B1)	NP_000488.3:p.Leu489=
NM_001026213.1:c.1267T>C (CYP11B1)	NP_001021384.1:p.Leu423=
ENST00000292427.8:c.1465T>C (CYP11B1)	ENSP00000292427.4:p.Leu489=
ENST00000314111.4:n.1662T>C (CYP11B1)
ENST00000377675.3:c.1678T>C (CYP11B1)	ENSP00000366903.3:p.Leu560=
ENST00000517471.5:c.1267T>C (CYP11B1)	ENSP00000428043.1:p.Leu423=
ENST00000519285.5:c.499T>C (CYP11B1)	ENSP00000430144.1:p.Leu167=
ENST00000522728.5:c.181+33195A>G (GML)	ENSP00000430799.1:n.181+33195A>G
XM_011516870.1:c.1703T>C (CYP11B1)	XP_011515172.1:p.Ile568Thr
XM_011516871.1:c.1634T>C (CYP11B1)	XP_011515173.1:p.Ile545Thr
XM_011516872.1:c.1625T>C (CYP11B1)	XP_011515174.1:p.Ile542Thr
XM_011516873.1:c.1612T>C (CYP11B1)	XP_011515175.1:p.Leu538=
XM_011516874.1:c.1543T>C (CYP11B1)	XP_011515176.1:p.Leu515=
XM_011516875.1:c.1442T>C (CYP11B1)	XP_011515177.1:p.Ile481Thr
XM_011516876.1:c.1414T>C (CYP11B1)	XP_011515178.1:p.Leu472=
XM_011516970.1:c.214+33195A>G (GML)	XP_011515272.1:n.214+33195A>G