Canonical Allele Identifier: CA1825497141

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142876610G= , CM000670.2:g.142876610G= GRCh38
NC_000008.10:g.143958026G= , CM000670.1:g.143958026G= GRCh37
NC_000008.9:g.143955028G= NCBI36
NG_007954.1:g.8211C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000292427.10:c.799+72C= (CYP11B1) MANE Select ENSP00000292427.5:n.799+72C=
ENST00000292427.8:c.799+72C= (CYP11B1) ENSP00000292427.4:n.799+72C=
ENST00000314111.4:n.832+72C= (CYP11B1)
ENST00000377675.3:c.1012+72C= (CYP11B1) ENSP00000366903.3:n.1012+72C=
ENST00000517471.5:c.799+72C= (CYP11B1) ENSP00000428043.1:n.799+72C=
ENST00000522728.5:c.181+35385G= (GML) ENSP00000430799.1:n.181+35385G=
NM_000497.3:c.799+72C= (CYP11B1) NP_000488.3:n.799+72C=
NM_001026213.1:c.799+72C= (CYP11B1) NP_001021384.1:n.799+72C=
XM_011516870.1:c.877+72C= (CYP11B1) XP_011515172.1:n.877+72C=
XM_011516871.1:c.877+72C= (CYP11B1) XP_011515173.1:n.877+72C=
XM_011516872.1:c.799+72C= (CYP11B1) XP_011515174.1:n.799+72C=
XM_011516873.1:c.877+72C= (CYP11B1) XP_011515175.1:n.877+72C=
XM_011516874.1:c.877+72C= (CYP11B1) XP_011515176.1:n.877+72C=
XM_011516875.1:c.616+72C= (CYP11B1) XP_011515177.1:n.616+72C=
XM_011516876.1:c.877+72C= (CYP11B1) XP_011515178.1:n.877+72C=
XM_011516970.1:c.214+35385G= (GML) XP_011515272.1:n.214+35385G=
NM_000497.4:c.799+72C= (CYP11B1) MANE Select NP_000488.3:n.799+72C=