Canonical Allele Identifier: CA1825496457

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142875542T= , CM000670.2:g.142875542T= GRCh38
NC_000008.10:g.143956958T= , CM000670.1:g.143956958T= GRCh37
NC_000008.9:g.143953960T= NCBI36
NG_007954.1:g.9279A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000292427.10:c.1121+170A= (CYP11B1) MANE Select ENSP00000292427.5:n.1121+170A=
ENST00000292427.8:c.1121+170A= (CYP11B1) ENSP00000292427.4:n.1121+170A=
ENST00000314111.4:n.1516+170A= (CYP11B1)
ENST00000377675.3:c.1334+170A= (CYP11B1) ENSP00000366903.3:n.1334+170A=
ENST00000517471.5:c.1121+170A= (CYP11B1) ENSP00000428043.1:n.1121+170A=
ENST00000519285.5:c.87-161A= (CYP11B1) ENSP00000430144.1:n.87-161A=
ENST00000522728.5:c.181+34317T= (GML) ENSP00000430799.1:n.181+34317T=
NM_000497.3:c.1121+170A= (CYP11B1) NP_000488.3:n.1121+170A=
NM_001026213.1:c.1121+170A= (CYP11B1) NP_001021384.1:n.1121+170A=
XM_011516870.1:c.1200-161A= (CYP11B1) XP_011515172.1:n.1200-161A=
XM_011516871.1:c.1199+170A= (CYP11B1) XP_011515173.1:n.1199+170A=
XM_011516872.1:c.1122-161A= (CYP11B1) XP_011515174.1:n.1122-161A=
XM_011516873.1:c.1200-161A= (CYP11B1) XP_011515175.1:n.1200-161A=
XM_011516874.1:c.1199+170A= (CYP11B1) XP_011515176.1:n.1199+170A=
XM_011516875.1:c.939-161A= (CYP11B1) XP_011515177.1:n.939-161A=
XM_011516876.1:c.1200-161A= (CYP11B1) XP_011515178.1:n.1200-161A=
XM_011516970.1:c.214+34317T= (GML) XP_011515272.1:n.214+34317T=
NM_000497.4:c.1121+170A= (CYP11B1) MANE Select NP_000488.3:n.1121+170A=