Canonical Allele Identifier: CA372390904

Gene: CYP11B1 GML

Linked Data

• MyVariant Identifiers: chr8:g.143955856T>G (hg19) ; chr8:g.142874440T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142874440T>G , CM000670.2:g.142874440T>G	GRCh38
NC_000008.10:g.143955856T>G , CM000670.1:g.143955856T>G	GRCh37
NC_000008.9:g.143952858T>G	NCBI36
NG_007954.1:g.10381A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000292427.10:c.1445A>C (CYP11B1) MANE Select	ENSP00000292427.5:p.Lys482Thr
ENST00000292427.8:c.1445A>C (CYP11B1)	ENSP00000292427.4:p.Lys482Thr
ENST00000314111.4:n.1642A>C (CYP11B1)
ENST00000377675.3:c.1658A>C (CYP11B1)	ENSP00000366903.3:p.Lys553Thr
ENST00000517471.5:c.1247A>C (CYP11B1)	ENSP00000428043.1:p.Lys416Thr
ENST00000519285.5:c.479A>C (CYP11B1)	ENSP00000430144.1:p.Lys160Thr
ENST00000522728.5:c.181+33215T>G (GML)	ENSP00000430799.1:n.181+33215T>G
NM_000497.3:c.1445A>C (CYP11B1)	NP_000488.3:p.Lys482Thr
NM_001026213.1:c.1247A>C (CYP11B1)	NP_001021384.1:p.Lys416Thr
XM_011516870.1:c.1683A>C (CYP11B1)	XP_011515172.1:p.Lys561Asn
XM_011516871.1:c.1614A>C (CYP11B1)	XP_011515173.1:p.Lys538Asn
XM_011516872.1:c.1605A>C (CYP11B1)	XP_011515174.1:p.Lys535Asn
XM_011516873.1:c.1592A>C (CYP11B1)	XP_011515175.1:p.Lys531Thr
XM_011516874.1:c.1523A>C (CYP11B1)	XP_011515176.1:p.Lys508Thr
XM_011516875.1:c.1422A>C (CYP11B1)	XP_011515177.1:p.Lys474Asn
XM_011516876.1:c.1394A>C (CYP11B1)	XP_011515178.1:p.Lys465Thr
XM_011516970.1:c.214+33215T>G (GML)	XP_011515272.1:n.214+33215T>G
NM_000497.4:c.1445A>C (CYP11B1) MANE Select	NP_000488.3:p.Lys482Thr