Canonical Allele Identifier: CA848694197

Linked Data

dbSNP Id: rs1246863389

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142911922del , CM000670.2:g.142911922del GRCh38
NC_000008.10:g.143993338del , CM000670.1:g.143993338del GRCh37
NC_000008.9:g.143990340del NCBI36
NG_008374.1:g.10922del

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.*58del (CYP11B2) MANE Select ENSP00000325822.2:n.*58del
ENST00000522728.5:c.182-2041del (GML) ENSP00000430799.1:n.182-2041del
NM_000498.3:c.*58del (CYP11B2) MANE Select NP_000489.3:n.*58del
XM_011516877.1:c.*58del (CYP11B2) XP_011515179.1:n.*58del
XM_011516878.1:c.*58del (CYP11B2) XP_011515180.1:n.*58del
XM_011516879.1:c.*58del (CYP11B2) XP_011515181.1:n.*58del
XM_011516970.1:c.215-2041del (GML) XP_011515272.1:n.215-2041del