Canonical Allele Identifier: CA4905290

Gene: CYP11B1 GML

Linked Data

• dbSNP Id: rs780265554
• ExAC: 8:143957799 A / G
• gnomAD v2: 8-143957799-A-G
• gnomAD v4: 8-142876383-A-G
• MyVariant Identifiers: chr8:g.143957799A>G (hg19) ; chr8:g.142876383A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142876383A>G , CM000670.2:g.142876383A>G	GRCh38
NC_000008.10:g.143957799A>G , CM000670.1:g.143957799A>G	GRCh37
NC_000008.9:g.143954801A>G	NCBI36
NG_007954.1:g.8438T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.812T>C (CYP11B1) MANE Select	ENSP00000292427.5:p.Ile271Thr
ENST00000292427.8:c.812T>C (CYP11B1)	ENSP00000292427.4:p.Ile271Thr
ENST00000314111.4:n.845T>C (CYP11B1)
ENST00000377675.3:c.1025T>C (CYP11B1)	ENSP00000366903.3:p.Ile342Thr
ENST00000517471.5:c.812T>C (CYP11B1)	ENSP00000428043.1:p.Ile271Thr
ENST00000522728.5:c.181+35158A>G (GML)	ENSP00000430799.1:n.181+35158A>G
NM_000497.3:c.812T>C (CYP11B1)	NP_000488.3:p.Ile271Thr
NM_001026213.1:c.812T>C (CYP11B1)	NP_001021384.1:p.Ile271Thr
XM_011516870.1:c.890T>C (CYP11B1)	XP_011515172.1:p.Ile297Thr
XM_011516871.1:c.890T>C (CYP11B1)	XP_011515173.1:p.Ile297Thr
XM_011516872.1:c.812T>C (CYP11B1)	XP_011515174.1:p.Ile271Thr
XM_011516873.1:c.890T>C (CYP11B1)	XP_011515175.1:p.Ile297Thr
XM_011516874.1:c.890T>C (CYP11B1)	XP_011515176.1:p.Ile297Thr
XM_011516875.1:c.629T>C (CYP11B1)	XP_011515177.1:p.Ile210Thr
XM_011516876.1:c.890T>C (CYP11B1)	XP_011515178.1:p.Ile297Thr
XM_011516970.1:c.214+35158A>G (GML)	XP_011515272.1:n.214+35158A>G
NM_000497.4:c.812T>C (CYP11B1) MANE Select	NP_000488.3:p.Ile271Thr