Canonical Allele Identifier: CA2688877195

Gene: CYP11B1 GML

Linked Data

• gnomAD v4: 8-142876069-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.142876069T>C , CM000670.2:g.142876069T>C	GRCh38
NC_000008.10:g.143957485T>C , CM000670.1:g.143957485T>C	GRCh37
NC_000008.9:g.143954487T>C	NCBI36
NG_007954.1:g.8752A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000292427.10:c.954+172A>G (CYP11B1) MANE Select	ENSP00000292427.5:n.954+172A>G
ENST00000292427.8:c.954+172A>G (CYP11B1)	ENSP00000292427.4:n.954+172A>G
ENST00000314111.4:n.1159A>G (CYP11B1)
ENST00000377675.3:c.1167+172A>G (CYP11B1)	ENSP00000366903.3:n.1167+172A>G
ENST00000517471.5:c.954+172A>G (CYP11B1)	ENSP00000428043.1:n.954+172A>G
ENST00000522728.5:c.181+34844T>C (GML)	ENSP00000430799.1:n.181+34844T>C
NM_000497.3:c.954+172A>G (CYP11B1)	NP_000488.3:n.954+172A>G
NM_001026213.1:c.954+172A>G (CYP11B1)	NP_001021384.1:n.954+172A>G
XM_011516870.1:c.1032+172A>G (CYP11B1)	XP_011515172.1:n.1032+172A>G
XM_011516871.1:c.1032+172A>G (CYP11B1)	XP_011515173.1:n.1032+172A>G
XM_011516872.1:c.954+172A>G (CYP11B1)	XP_011515174.1:n.954+172A>G
XM_011516873.1:c.1032+172A>G (CYP11B1)	XP_011515175.1:n.1032+172A>G
XM_011516874.1:c.1032+172A>G (CYP11B1)	XP_011515176.1:n.1032+172A>G
XM_011516875.1:c.771+172A>G (CYP11B1)	XP_011515177.1:n.771+172A>G
XM_011516876.1:c.1032+172A>G (CYP11B1)	XP_011515178.1:n.1032+172A>G
XM_011516970.1:c.214+34844T>C (GML)	XP_011515272.1:n.214+34844T>C
NM_000497.4:c.954+172A>G (CYP11B1) MANE Select	NP_000488.3:n.954+172A>G