Canonical Allele Identifier: CA372396483

Linked Data

dbSNP Id: rs1383107624

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142879063G>T , CM000670.2:g.142879063G>T GRCh38
NC_000008.10:g.143960479G>T , CM000670.1:g.143960479G>T GRCh37
NC_000008.9:g.143957481G>T NCBI36
NG_007954.1:g.5758C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000292427.10:c.364C>A (CYP11B1) MANE Select ENSP00000292427.5:p.His122Asn
ENST00000292427.8:c.364C>A (CYP11B1) ENSP00000292427.4:p.His122Asn
ENST00000314111.4:n.397C>A (CYP11B1)
ENST00000377675.3:c.499C>A (CYP11B1) ENSP00000366903.3:p.His167Asn
ENST00000517471.5:c.364C>A (CYP11B1) ENSP00000428043.1:p.His122Asn
ENST00000522728.5:c.182-34900G>T (GML) ENSP00000430799.1:n.182-34900G>T
NM_000497.3:c.364C>A (CYP11B1) NP_000488.3:p.His122Asn
NM_001026213.1:c.364C>A (CYP11B1) NP_001021384.1:p.His122Asn
XM_011516870.1:c.364C>A (CYP11B1) XP_011515172.1:p.His122Asn
XM_011516871.1:c.364C>A (CYP11B1) XP_011515173.1:p.His122Asn
XM_011516872.1:c.364C>A (CYP11B1) XP_011515174.1:p.His122Asn
XM_011516873.1:c.364C>A (CYP11B1) XP_011515175.1:p.His122Asn
XM_011516874.1:c.364C>A (CYP11B1) XP_011515176.1:p.His122Asn
XM_011516875.1:c.103C>A (CYP11B1) XP_011515177.1:p.His35Asn
XM_011516876.1:c.364C>A (CYP11B1) XP_011515178.1:p.His122Asn
XM_011516970.1:c.215-34900G>T (GML) XP_011515272.1:n.215-34900G>T
NM_000497.4:c.364C>A (CYP11B1) MANE Select NP_000488.3:p.His122Asn