Canonical Allele Identifier: CA2688875873

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142912462_142912481dup , CM000670.2:g.142912462_142912481dup GRCh38
NC_000008.10:g.143993878_143993897dup , CM000670.1:g.143993878_143993897dup GRCh37
NC_000008.9:g.143990880_143990899dup NCBI36
NG_008374.1:g.10364_10383dup

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.1398+50_1398+69dup (CYP11B2) MANE Select ENSP00000325822.2:n.1398+50_1398+69dup
ENST00000522728.5:c.182-1501_182-1482dup (GML) ENSP00000430799.1:n.182-1501_182-1482dup
NM_000498.3:c.1398+50_1398+69dup (CYP11B2) MANE Select NP_000489.3:n.1398+50_1398+69dup
XM_011516877.1:c.1545+50_1545+69dup (CYP11B2) XP_011515179.1:n.1545+50_1545+69dup
XM_011516878.1:c.1476+50_1476+69dup (CYP11B2) XP_011515180.1:n.1476+50_1476+69dup
XM_011516879.1:c.1467+50_1467+69dup (CYP11B2) XP_011515181.1:n.1467+50_1467+69dup
XM_011516970.1:c.215-1501_215-1482dup (GML) XP_011515272.1:n.215-1501_215-1482dup