Canonical Allele Identifier: CA1825495789

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142874434A= , CM000670.2:g.142874434A= GRCh38
NC_000008.10:g.143955850A= , CM000670.1:g.143955850A= GRCh37
NC_000008.9:g.143952852A= NCBI36
NG_007954.1:g.10387T=

Transcript Alleles

HGVS Amino-acid change
ENST00000292427.10:c.1451T= (CYP11B1) MANE Select ENSP00000292427.5:p.Val484=
ENST00000292427.8:c.1451T= (CYP11B1) ENSP00000292427.4:p.Val484=
ENST00000314111.4:n.1648T= (CYP11B1)
ENST00000377675.3:c.1664T= (CYP11B1) ENSP00000366903.3:p.Val555=
ENST00000517471.5:c.1253T= (CYP11B1) ENSP00000428043.1:p.Val418=
ENST00000519285.5:c.485T= (CYP11B1) ENSP00000430144.1:p.Val162=
ENST00000522728.5:c.181+33209A= (GML) ENSP00000430799.1:n.181+33209A=
NM_000497.3:c.1451T= (CYP11B1) NP_000488.3:p.Val484=
NM_001026213.1:c.1253T= (CYP11B1) NP_001021384.1:p.Val418=
XM_011516870.1:c.1689T= (CYP11B1) XP_011515172.1:p.Gly563=
XM_011516871.1:c.1620T= (CYP11B1) XP_011515173.1:p.Gly540=
XM_011516872.1:c.1611T= (CYP11B1) XP_011515174.1:p.Gly537=
XM_011516873.1:c.1598T= (CYP11B1) XP_011515175.1:p.Val533=
XM_011516874.1:c.1529T= (CYP11B1) XP_011515176.1:p.Val510=
XM_011516875.1:c.1428T= (CYP11B1) XP_011515177.1:p.Gly476=
XM_011516876.1:c.1400T= (CYP11B1) XP_011515178.1:p.Val467=
XM_011516970.1:c.214+33209A= (GML) XP_011515272.1:n.214+33209A=
NM_000497.4:c.1451T= (CYP11B1) MANE Select NP_000488.3:p.Val484=