Canonical Allele Identifier: CA4905161

Gene: CYP11B1 GML

Linked Data

• dbSNP Id: rs764827972
• ExAC: 8:143957162 G / C
• gnomAD v2: 8-143957162-G-C
• gnomAD v4: 8-142875746-G-C
• MyVariant Identifiers: chr8:g.143957162G>C (hg19) ; chr8:g.142875746G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142875746G>C , CM000670.2:g.142875746G>C	GRCh38
NC_000008.10:g.143957162G>C , CM000670.1:g.143957162G>C	GRCh37
NC_000008.9:g.143954164G>C	NCBI36
NG_007954.1:g.9075C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.1087C>G (CYP11B1) MANE Select	ENSP00000292427.5:p.Pro363Ala
ENST00000292427.8:c.1087C>G (CYP11B1)	ENSP00000292427.4:p.Pro363Ala
ENST00000314111.4:n.1482C>G (CYP11B1)
ENST00000377675.3:c.1300C>G (CYP11B1)	ENSP00000366903.3:p.Pro434Ala
ENST00000517471.5:c.1087C>G (CYP11B1)	ENSP00000428043.1:p.Pro363Ala
ENST00000519285.5:c.52C>G (CYP11B1)	ENSP00000430144.1:p.Pro18Ala
ENST00000522728.5:c.181+34521G>C (GML)	ENSP00000430799.1:n.181+34521G>C
NM_000497.3:c.1087C>G (CYP11B1)	NP_000488.3:p.Pro363Ala
NM_001026213.1:c.1087C>G (CYP11B1)	NP_001021384.1:p.Pro363Ala
XM_011516870.1:c.1165C>G (CYP11B1)	XP_011515172.1:p.Pro389Ala
XM_011516871.1:c.1165C>G (CYP11B1)	XP_011515173.1:p.Pro389Ala
XM_011516872.1:c.1087C>G (CYP11B1)	XP_011515174.1:p.Pro363Ala
XM_011516873.1:c.1165C>G (CYP11B1)	XP_011515175.1:p.Pro389Ala
XM_011516874.1:c.1165C>G (CYP11B1)	XP_011515176.1:p.Pro389Ala
XM_011516875.1:c.904C>G (CYP11B1)	XP_011515177.1:p.Pro302Ala
XM_011516876.1:c.1165C>G (CYP11B1)	XP_011515178.1:p.Pro389Ala
XM_011516970.1:c.214+34521G>C (GML)	XP_011515272.1:n.214+34521G>C
NM_000497.4:c.1087C>G (CYP11B1) MANE Select	NP_000488.3:p.Pro363Ala