Canonical Allele Identifier: CA1825495793

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142874444T= , CM000670.2:g.142874444T= GRCh38
NC_000008.10:g.143955860T= , CM000670.1:g.143955860T= GRCh37
NC_000008.9:g.143952862T= NCBI36
NG_007954.1:g.10377A=

Transcript Alleles

HGVS Amino-acid change
ENST00000292427.10:c.1441A= (CYP11B1) MANE Select ENSP00000292427.5:p.Ile481=
ENST00000292427.8:c.1441A= (CYP11B1) ENSP00000292427.4:p.Ile481=
ENST00000314111.4:n.1638A= (CYP11B1)
ENST00000377675.3:c.1654A= (CYP11B1) ENSP00000366903.3:p.Ile552=
ENST00000517471.5:c.1243A= (CYP11B1) ENSP00000428043.1:p.Ile415=
ENST00000519285.5:c.475A= (CYP11B1) ENSP00000430144.1:p.Ile159=
ENST00000522728.5:c.181+33219T= (GML) ENSP00000430799.1:n.181+33219T=
NM_000497.3:c.1441A= (CYP11B1) NP_000488.3:p.Ile481=
NM_001026213.1:c.1243A= (CYP11B1) NP_001021384.1:p.Ile415=
XM_011516870.1:c.1679A= (CYP11B1) XP_011515172.1:p.His560=
XM_011516871.1:c.1610A= (CYP11B1) XP_011515173.1:p.His537=
XM_011516872.1:c.1601A= (CYP11B1) XP_011515174.1:p.His534=
XM_011516873.1:c.1588A= (CYP11B1) XP_011515175.1:p.Ile530=
XM_011516874.1:c.1519A= (CYP11B1) XP_011515176.1:p.Ile507=
XM_011516875.1:c.1418A= (CYP11B1) XP_011515177.1:p.His473=
XM_011516876.1:c.1390A= (CYP11B1) XP_011515178.1:p.Ile464=
XM_011516970.1:c.214+33219T= (GML) XP_011515272.1:n.214+33219T=
NM_000497.4:c.1441A= (CYP11B1) MANE Select NP_000488.3:p.Ile481=