Canonical Allele Identifier: CA1825514110

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142911921_142911922delinsCT , CM000670.2:g.142911921_142911922delinsCT GRCh38
NC_000008.10:g.143993337_143993338delinsCT , CM000670.1:g.143993337_143993338delinsCT GRCh37
NC_000008.9:g.143990339_143990340delinsCT NCBI36
NG_008374.1:g.10922_10923delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.*58_*59delinsAG (CYP11B2) MANE Select ENSP00000325822.2:n.*58_*59delinsAG
ENST00000522728.5:c.182-2042_182-2041delinsCT (GML) ENSP00000430799.1:n.182-2042_182-2041deli...
NM_000498.3:c.*58_*59delinsAG (CYP11B2) MANE Select NP_000489.3:n.*58_*59delinsAG
XM_011516877.1:c.*58_*59delinsAG (CYP11B2) XP_011515179.1:n.*58_*59delinsAG
XM_011516878.1:c.*58_*59delinsAG (CYP11B2) XP_011515180.1:n.*58_*59delinsAG
XM_011516879.1:c.*58_*59delinsAG (CYP11B2) XP_011515181.1:n.*58_*59delinsAG
XM_011516970.1:c.215-2042_215-2041delinsCT (GML) XP_011515272.1:n.215-2042_215-2041delinsC...