Canonical Allele Identifier: CA372395408

Gene: CYP11B1 GML

Linked Data

• gnomAD v4: 8-142876697-A-G
• MyVariant Identifiers: chr8:g.143958113A>G (hg19) ; chr8:g.142876697A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142876697A>G , CM000670.2:g.142876697A>G	GRCh38
NC_000008.10:g.143958113A>G , CM000670.1:g.143958113A>G	GRCh37
NC_000008.9:g.143955115A>G	NCBI36
NG_007954.1:g.8124T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.784T>C (CYP11B1) MANE Select	ENSP00000292427.5:p.Cys262Arg
ENST00000292427.8:c.784T>C (CYP11B1)	ENSP00000292427.4:p.Cys262Arg
ENST00000314111.4:n.817T>C (CYP11B1)
ENST00000377675.3:c.997T>C (CYP11B1)	ENSP00000366903.3:p.Cys333Arg
ENST00000517471.5:c.784T>C (CYP11B1)	ENSP00000428043.1:p.Cys262Arg
ENST00000522728.5:c.181+35472A>G (GML)	ENSP00000430799.1:n.181+35472A>G
NM_000497.3:c.784T>C (CYP11B1)	NP_000488.3:p.Cys262Arg
NM_001026213.1:c.784T>C (CYP11B1)	NP_001021384.1:p.Cys262Arg
XM_011516870.1:c.862T>C (CYP11B1)	XP_011515172.1:p.Cys288Arg
XM_011516871.1:c.862T>C (CYP11B1)	XP_011515173.1:p.Cys288Arg
XM_011516872.1:c.784T>C (CYP11B1)	XP_011515174.1:p.Cys262Arg
XM_011516873.1:c.862T>C (CYP11B1)	XP_011515175.1:p.Cys288Arg
XM_011516874.1:c.862T>C (CYP11B1)	XP_011515176.1:p.Cys288Arg
XM_011516875.1:c.601T>C (CYP11B1)	XP_011515177.1:p.Cys201Arg
XM_011516876.1:c.862T>C (CYP11B1)	XP_011515178.1:p.Cys288Arg
XM_011516970.1:c.214+35472A>G (GML)	XP_011515272.1:n.214+35472A>G
NM_000497.4:c.784T>C (CYP11B1) MANE Select	NP_000488.3:p.Cys262Arg