Canonical Allele Identifier: CA1825514466

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142912547G= , CM000670.2:g.142912547G= GRCh38
NC_000008.10:g.143993963G= , CM000670.1:g.143993963G= GRCh37
NC_000008.9:g.143990965G= NCBI36
NG_008374.1:g.10297C=

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.1381C= (CYP11B2) MANE Select ENSP00000325822.2:p.Leu461=
ENST00000522728.5:c.182-1416G= (GML) ENSP00000430799.1:n.182-1416G=
NM_000498.3:c.1381C= (CYP11B2) MANE Select NP_000489.3:p.Leu461=
XM_011516877.1:c.1528C= (CYP11B2) XP_011515179.1:p.Leu510=
XM_011516878.1:c.1459C= (CYP11B2) XP_011515180.1:p.Leu487=
XM_011516879.1:c.1450C= (CYP11B2) XP_011515181.1:p.Leu484=
XM_011516970.1:c.215-1416G= (GML) XP_011515272.1:n.215-1416G=