Canonical Allele Identifier: CA372385957

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142912552T>G , CM000670.2:g.142912552T>G GRCh38
NC_000008.10:g.143993968T>G , CM000670.1:g.143993968T>G GRCh37
NC_000008.9:g.143990970T>G NCBI36
NG_008374.1:g.10292A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.1376A>C (CYP11B2) MANE Select ENSP00000325822.2:p.Glu459Ala
ENST00000522728.5:c.182-1411T>G (GML) ENSP00000430799.1:n.182-1411T>G
NM_000498.3:c.1376A>C (CYP11B2) MANE Select NP_000489.3:p.Glu459Ala
XM_011516877.1:c.1523A>C (CYP11B2) XP_011515179.1:p.Glu508Ala
XM_011516878.1:c.1454A>C (CYP11B2) XP_011515180.1:p.Glu485Ala
XM_011516879.1:c.1445A>C (CYP11B2) XP_011515181.1:p.Glu482Ala
XM_011516970.1:c.215-1411T>G (GML) XP_011515272.1:n.215-1411T>G