Canonical Allele Identifier: CA1825514472

Linked Data

dbSNP Id: rs1817555059

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142912556_142912557dup , CM000670.2:g.142912556_142912557dup GRCh38
NC_000008.10:g.143993972_143993973dup , CM000670.1:g.143993972_143993973dup GRCh37
NC_000008.9:g.143990974_143990975dup NCBI36
NG_008374.1:g.10287_10288dup

Transcript Alleles

HGVS Amino-acid change
ENST00000323110.2:c.1371_1372dup (CYP11B2) MANE Select ENSP00000325822.2:p.Ala458GlyfsTer12
ENST00000522728.5:c.182-1407_182-1406dup (GML) ENSP00000430799.1:n.182-1407_182-1406dup
NM_000498.3:c.1371_1372dup (CYP11B2) MANE Select NP_000489.3:p.Ala458GlyfsTer12
XM_011516877.1:c.1518_1519dup (CYP11B2) XP_011515179.1:p.Ala507GlyfsTer12
XM_011516878.1:c.1449_1450dup (CYP11B2) XP_011515180.1:p.Ala484GlyfsTer12
XM_011516879.1:c.1440_1441dup (CYP11B2) XP_011515181.1:p.Ala481GlyfsTer12
XM_011516970.1:c.215-1407_215-1406dup (GML) XP_011515272.1:n.215-1407_215-1406dup