Canonical Allele Identifier: CA372390824

Gene: CYP11B1 GML

Linked Data

• gnomAD v4: 8-142874426-A-G
• MyVariant Identifiers: chr8:g.143955842A>G (hg19) ; chr8:g.142874426A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142874426A>G , CM000670.2:g.142874426A>G	GRCh38
NC_000008.10:g.143955842A>G , CM000670.1:g.143955842A>G	GRCh37
NC_000008.9:g.143952844A>G	NCBI36
NG_007954.1:g.10395T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.1459T>C (CYP11B1) MANE Select	ENSP00000292427.5:p.Phe487Leu
ENST00000292427.8:c.1459T>C (CYP11B1)	ENSP00000292427.4:p.Phe487Leu
ENST00000314111.4:n.1656T>C (CYP11B1)
ENST00000377675.3:c.1672T>C (CYP11B1)	ENSP00000366903.3:p.Phe558Leu
ENST00000517471.5:c.1261T>C (CYP11B1)	ENSP00000428043.1:p.Phe421Leu
ENST00000519285.5:c.493T>C (CYP11B1)	ENSP00000430144.1:p.Phe165Leu
ENST00000522728.5:c.181+33201A>G (GML)	ENSP00000430799.1:n.181+33201A>G
NM_000497.3:c.1459T>C (CYP11B1)	NP_000488.3:p.Phe487Leu
NM_001026213.1:c.1261T>C (CYP11B1)	NP_001021384.1:p.Phe421Leu
XM_011516870.1:c.1697T>C (CYP11B1)	XP_011515172.1:p.Leu566Pro
XM_011516871.1:c.1628T>C (CYP11B1)	XP_011515173.1:p.Leu543Pro
XM_011516872.1:c.1619T>C (CYP11B1)	XP_011515174.1:p.Leu540Pro
XM_011516873.1:c.1606T>C (CYP11B1)	XP_011515175.1:p.Phe536Leu
XM_011516874.1:c.1537T>C (CYP11B1)	XP_011515176.1:p.Phe513Leu
XM_011516875.1:c.1436T>C (CYP11B1)	XP_011515177.1:p.Leu479Pro
XM_011516876.1:c.1408T>C (CYP11B1)	XP_011515178.1:p.Phe470Leu
XM_011516970.1:c.214+33201A>G (GML)	XP_011515272.1:n.214+33201A>G
NM_000497.4:c.1459T>C (CYP11B1) MANE Select	NP_000488.3:p.Phe487Leu