Canonical Allele Identifier: CA4905110

Gene: CYP11B1 GML

Linked Data

• dbSNP Id: rs61752793
• ExAC: 8:143956769 T / C
• gnomAD v2: 8-143956769-T-C
• gnomAD v3: 8-142875353-T-C
• gnomAD v4: 8-142875353-T-C
• MyVariant Identifiers: chr8:g.143956769T>C (hg19) ; chr8:g.142875353T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142875353T>C , CM000670.2:g.142875353T>C	GRCh38
NC_000008.10:g.143956769T>C , CM000670.1:g.143956769T>C	GRCh37
NC_000008.9:g.143953771T>C	NCBI36
NG_007954.1:g.9468A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.1122-41A>G (CYP11B1) MANE Select	ENSP00000292427.5:n.1122-41A>G
ENST00000292427.8:c.1122-41A>G (CYP11B1)	ENSP00000292427.4:n.1122-41A>G
ENST00000314111.4:n.1517-41A>G (CYP11B1)
ENST00000377675.3:c.1335-41A>G (CYP11B1)	ENSP00000366903.3:n.1335-41A>G
ENST00000517471.5:c.1122-41A>G (CYP11B1)	ENSP00000428043.1:n.1122-41A>G
ENST00000519285.5:c.115A>G (CYP11B1)	ENSP00000430144.1:p.Ile39Val
ENST00000522728.5:c.181+34128T>C (GML)	ENSP00000430799.1:n.181+34128T>C
NM_000497.3:c.1122-41A>G (CYP11B1)	NP_000488.3:n.1122-41A>G
NM_001026213.1:c.1122-41A>G (CYP11B1)	NP_001021384.1:n.1122-41A>G
XM_011516870.1:c.1228A>G (CYP11B1)	XP_011515172.1:p.Ile410Val
XM_011516871.1:c.1200-41A>G (CYP11B1)	XP_011515173.1:n.1200-41A>G
XM_011516872.1:c.1150A>G (CYP11B1)	XP_011515174.1:p.Ile384Val
XM_011516873.1:c.1228A>G (CYP11B1)	XP_011515175.1:p.Ile410Val
XM_011516874.1:c.1200-41A>G (CYP11B1)	XP_011515176.1:n.1200-41A>G
XM_011516875.1:c.967A>G (CYP11B1)	XP_011515177.1:p.Ile323Val
XM_011516876.1:c.1228A>G (CYP11B1)	XP_011515178.1:p.Ile410Val
XM_011516970.1:c.214+34128T>C (GML)	XP_011515272.1:n.214+34128T>C
NM_000497.4:c.1122-41A>G (CYP11B1) MANE Select	NP_000488.3:n.1122-41A>G