Canonical Allele Identifier: CA1825514469

Linked Data

dbSNP Id: rs1817554855

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142912558_142912563del , CM000670.2:g.142912558_142912563del GRCh38
NC_000008.10:g.143993974_143993979del , CM000670.1:g.143993974_143993979del GRCh37
NC_000008.9:g.143990976_143990981del NCBI36
NG_008374.1:g.10288_10293del

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.1372_1377del (CYP11B2) MANE Select ENSP00000325822.2:p.Ala458_Glu459del
ENST00000522728.5:c.182-1405_182-1400del (GML) ENSP00000430799.1:n.182-1405_182-1400del
NM_000498.3:c.1372_1377del (CYP11B2) MANE Select NP_000489.3:p.Ala458_Glu459del
XM_011516877.1:c.1519_1524del (CYP11B2) XP_011515179.1:p.Ala507_Glu508del
XM_011516878.1:c.1450_1455del (CYP11B2) XP_011515180.1:p.Ala484_Glu485del
XM_011516879.1:c.1441_1446del (CYP11B2) XP_011515181.1:p.Ala481_Glu482del
XM_011516970.1:c.215-1405_215-1400del (GML) XP_011515272.1:n.215-1405_215-1400del