Canonical Allele Identifier: CA372395076

Gene: CYP11B1 GML

Linked Data

• dbSNP Id: rs1816944558
• gnomAD v4: 8-142876258-C-T
• COSMIC: COSM1096876
• MyVariant Identifiers: chr8:g.143957674C>T (hg19) ; chr8:g.142876258C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142876258C>T , CM000670.2:g.142876258C>T	GRCh38
NC_000008.10:g.143957674C>T , CM000670.1:g.143957674C>T	GRCh37
NC_000008.9:g.143954676C>T	NCBI36
NG_007954.1:g.8563G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000292427.10:c.937G>A (CYP11B1) MANE Select	ENSP00000292427.5:p.Ala313Thr
ENST00000292427.8:c.937G>A (CYP11B1)	ENSP00000292427.4:p.Ala313Thr
ENST00000314111.4:n.970G>A (CYP11B1)
ENST00000377675.3:c.1150G>A (CYP11B1)	ENSP00000366903.3:p.Ala384Thr
ENST00000517471.5:c.937G>A (CYP11B1)	ENSP00000428043.1:p.Ala313Thr
ENST00000522728.5:c.181+35033C>T (GML)	ENSP00000430799.1:n.181+35033C>T
NM_000497.3:c.937G>A (CYP11B1)	NP_000488.3:p.Ala313Thr
NM_001026213.1:c.937G>A (CYP11B1)	NP_001021384.1:p.Ala313Thr
XM_011516870.1:c.1015G>A (CYP11B1)	XP_011515172.1:p.Ala339Thr
XM_011516871.1:c.1015G>A (CYP11B1)	XP_011515173.1:p.Ala339Thr
XM_011516872.1:c.937G>A (CYP11B1)	XP_011515174.1:p.Ala313Thr
XM_011516873.1:c.1015G>A (CYP11B1)	XP_011515175.1:p.Ala339Thr
XM_011516874.1:c.1015G>A (CYP11B1)	XP_011515176.1:p.Ala339Thr
XM_011516875.1:c.754G>A (CYP11B1)	XP_011515177.1:p.Ala252Thr
XM_011516876.1:c.1015G>A (CYP11B1)	XP_011515178.1:p.Ala339Thr
XM_011516970.1:c.214+35033C>T (GML)	XP_011515272.1:n.214+35033C>T
NM_000497.4:c.937G>A (CYP11B1) MANE Select	NP_000488.3:p.Ala313Thr