Canonical Allele Identifier: CA463324908

Gene: CYP11B1 GML

Linked Data

• MyVariant Identifiers: chr8:g.143955810G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142874394G>A , CM000670.2:g.142874394G>A	GRCh38
NC_000008.10:g.143955810G>A , CM000670.1:g.143955810G>A	GRCh37
NC_000008.9:g.143952812G>A	NCBI36
NG_007954.1:g.10427C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.1491C>T (CYP11B1) MANE Select	ENSP00000292427.5:p.Leu497=
ENST00000292427.8:c.1491C>T (CYP11B1)	ENSP00000292427.4:p.Leu497=
ENST00000314111.4:n.1688C>T (CYP11B1)
ENST00000377675.3:c.1704C>T (CYP11B1)	ENSP00000366903.3:p.Leu568=
ENST00000517471.5:c.1293C>T (CYP11B1)	ENSP00000428043.1:p.Leu431=
ENST00000519285.5:c.525C>T (CYP11B1)	ENSP00000430144.1:p.Leu175=
ENST00000522728.5:c.181+33169G>A (GML)	ENSP00000430799.1:n.181+33169G>A
NM_000497.3:c.1491C>T (CYP11B1)	NP_000488.3:p.Leu497=
NM_001026213.1:c.1293C>T (CYP11B1)	NP_001021384.1:p.Leu431=
XM_011516870.1:c.1729C>T (CYP11B1)	XP_011515172.1:p.His577Tyr
XM_011516871.1:c.1660C>T (CYP11B1)	XP_011515173.1:p.His554Tyr
XM_011516872.1:c.1651C>T (CYP11B1)	XP_011515174.1:p.His551Tyr
XM_011516873.1:c.1638C>T (CYP11B1)	XP_011515175.1:p.Leu546=
XM_011516874.1:c.1569C>T (CYP11B1)	XP_011515176.1:p.Leu523=
XM_011516875.1:c.1468C>T (CYP11B1)	XP_011515177.1:p.His490Tyr
XM_011516876.1:c.1440C>T (CYP11B1)	XP_011515178.1:p.Leu480=
XM_011516970.1:c.214+33169G>A (GML)	XP_011515272.1:n.214+33169G>A
NM_000497.4:c.1491C>T (CYP11B1) MANE Select	NP_000488.3:p.Leu497=