Canonical Allele Identifier: CA372390659

Gene: CYP11B1 GML

Linked Data

• MyVariant Identifiers: chr8:g.143955817G>C (hg19) ; chr8:g.142874401G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142874401G>C , CM000670.2:g.142874401G>C	GRCh38
NC_000008.10:g.143955817G>C , CM000670.1:g.143955817G>C	GRCh37
NC_000008.9:g.143952819G>C	NCBI36
NG_007954.1:g.10420C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.1484C>G (CYP11B1) MANE Select	ENSP00000292427.5:p.Pro495Arg
ENST00000292427.8:c.1484C>G (CYP11B1)	ENSP00000292427.4:p.Pro495Arg
ENST00000314111.4:n.1681C>G (CYP11B1)
ENST00000377675.3:c.1697C>G (CYP11B1)	ENSP00000366903.3:p.Pro566Arg
ENST00000517471.5:c.1286C>G (CYP11B1)	ENSP00000428043.1:p.Pro429Arg
ENST00000519285.5:c.518C>G (CYP11B1)	ENSP00000430144.1:p.Pro173Arg
ENST00000522728.5:c.181+33176G>C (GML)	ENSP00000430799.1:n.181+33176G>C
NM_000497.3:c.1484C>G (CYP11B1)	NP_000488.3:p.Pro495Arg
NM_001026213.1:c.1286C>G (CYP11B1)	NP_001021384.1:p.Pro429Arg
XM_011516870.1:c.1722C>G (CYP11B1)	XP_011515172.1:p.Pro574=
XM_011516871.1:c.1653C>G (CYP11B1)	XP_011515173.1:p.Pro551=
XM_011516872.1:c.1644C>G (CYP11B1)	XP_011515174.1:p.Pro548=
XM_011516873.1:c.1631C>G (CYP11B1)	XP_011515175.1:p.Pro544Arg
XM_011516874.1:c.1562C>G (CYP11B1)	XP_011515176.1:p.Pro521Arg
XM_011516875.1:c.1461C>G (CYP11B1)	XP_011515177.1:p.Pro487=
XM_011516876.1:c.1433C>G (CYP11B1)	XP_011515178.1:p.Pro478Arg
XM_011516970.1:c.214+33176G>C (GML)	XP_011515272.1:n.214+33176G>C
NM_000497.4:c.1484C>G (CYP11B1) MANE Select	NP_000488.3:p.Pro495Arg