Canonical Allele Identifier: CA463324900

Gene: CYP11B1 GML

Linked Data

• MyVariant Identifiers: chr8:g.143955807G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142874391G>C , CM000670.2:g.142874391G>C	GRCh38
NC_000008.10:g.143955807G>C , CM000670.1:g.143955807G>C	GRCh37
NC_000008.9:g.143952809G>C	NCBI36
NG_007954.1:g.10430C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.1494C>G (CYP11B1) MANE Select	ENSP00000292427.5:p.Thr498=
ENST00000292427.8:c.1494C>G (CYP11B1)	ENSP00000292427.4:p.Thr498=
ENST00000314111.4:n.1691C>G (CYP11B1)
ENST00000377675.3:c.1707C>G (CYP11B1)	ENSP00000366903.3:p.Thr569=
ENST00000517471.5:c.1296C>G (CYP11B1)	ENSP00000428043.1:p.Thr432=
ENST00000519285.5:c.528C>G (CYP11B1)	ENSP00000430144.1:p.Thr176=
ENST00000522728.5:c.181+33166G>C (GML)	ENSP00000430799.1:n.181+33166G>C
NM_000497.3:c.1494C>G (CYP11B1)	NP_000488.3:p.Thr498=
NM_001026213.1:c.1296C>G (CYP11B1)	NP_001021384.1:p.Thr432=
XM_011516870.1:c.1732C>G (CYP11B1)	XP_011515172.1:p.Leu578Val
XM_011516871.1:c.1663C>G (CYP11B1)	XP_011515173.1:p.Leu555Val
XM_011516872.1:c.1654C>G (CYP11B1)	XP_011515174.1:p.Leu552Val
XM_011516873.1:c.1641C>G (CYP11B1)	XP_011515175.1:p.Thr547=
XM_011516874.1:c.1572C>G (CYP11B1)	XP_011515176.1:p.Thr524=
XM_011516875.1:c.1471C>G (CYP11B1)	XP_011515177.1:p.Leu491Val
XM_011516876.1:c.1443C>G (CYP11B1)	XP_011515178.1:p.Thr481=
XM_011516970.1:c.214+33166G>C (GML)	XP_011515272.1:n.214+33166G>C
NM_000497.4:c.1494C>G (CYP11B1) MANE Select	NP_000488.3:p.Thr498=