Canonical Allele Identifier: CA1825495795

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142874446T= , CM000670.2:g.142874446T= GRCh38
NC_000008.10:g.143955862T= , CM000670.1:g.143955862T= GRCh37
NC_000008.9:g.143952864T= NCBI36
NG_007954.1:g.10375A=

Transcript Alleles

HGVS Amino-acid change
ENST00000292427.10:c.1439A= (CYP11B1) MANE Select ENSP00000292427.5:p.Asp480=
ENST00000292427.8:c.1439A= (CYP11B1) ENSP00000292427.4:p.Asp480=
ENST00000314111.4:n.1636A= (CYP11B1)
ENST00000377675.3:c.1652A= (CYP11B1) ENSP00000366903.3:p.Asp551=
ENST00000517471.5:c.1241A= (CYP11B1) ENSP00000428043.1:p.Asp414=
ENST00000519285.5:c.473A= (CYP11B1) ENSP00000430144.1:p.Asp158=
ENST00000522728.5:c.181+33221T= (GML) ENSP00000430799.1:n.181+33221T=
NM_000497.3:c.1439A= (CYP11B1) NP_000488.3:p.Asp480=
NM_001026213.1:c.1241A= (CYP11B1) NP_001021384.1:p.Asp414=
XM_011516870.1:c.1677A= (CYP11B1) XP_011515172.1:p.Gly559=
XM_011516871.1:c.1608A= (CYP11B1) XP_011515173.1:p.Gly536=
XM_011516872.1:c.1599A= (CYP11B1) XP_011515174.1:p.Gly533=
XM_011516873.1:c.1586A= (CYP11B1) XP_011515175.1:p.Asp529=
XM_011516874.1:c.1517A= (CYP11B1) XP_011515176.1:p.Asp506=
XM_011516875.1:c.1416A= (CYP11B1) XP_011515177.1:p.Gly472=
XM_011516876.1:c.1388A= (CYP11B1) XP_011515178.1:p.Asp463=
XM_011516970.1:c.214+33221T= (GML) XP_011515272.1:n.214+33221T=
NM_000497.4:c.1439A= (CYP11B1) MANE Select NP_000488.3:p.Asp480=