Canonical Allele Identifier: CA8946037
Gene: SETBP1 HGNC NCBI

Linked Data

dbSNP Id: rs758450543

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.44953319T>C , CM000680.2:g.44953319T>C GRCh38
NC_000018.9:g.42533284T>C , CM000680.1:g.42533284T>C GRCh37
NC_000018.8:g.40787282T>C NCBI36
NG_027527.1:g.278147T>C
NG_027527.2:g.278147T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000649279.2:c.3979T>C MANE Select ENSP00000497406.1:p.Tyr1327His
ENST00000677068.1:c.3979T>C ENSP00000504398.1:p.Tyr1327His
ENST00000677077.1:c.3979T>C ENSP00000503656.1:p.Tyr1327His
ENST00000677130.1:c.3979T>C ENSP00000503094.1:p.Tyr1327His
ENST00000677699.1:c.3979T>C ENSP00000503964.1:p.Tyr1327His
ENST00000678152.1:c.3979T>C ENSP00000502995.1:p.Tyr1327His
ENST00000282030.5:c.3979T>C ENSP00000282030.5:p.Tyr1327His
NM_015559.2:c.3979T>C NP_056374.2:p.Tyr1327His
XM_005258243.3:c.3979T>C XP_005258300.1:p.Tyr1327His
NM_015559.3:c.3979T>C MANE Select NP_056374.2:p.Tyr1327His
XM_024451149.1:c.4057T>C XP_024306917.1:p.Tyr1353His
XM_024451150.1:c.4057T>C XP_024306918.1:p.Tyr1353His
XM_024451151.1:c.4057T>C XP_024306919.1:p.Tyr1353His
XM_024451152.1:c.4057T>C XP_024306920.1:p.Tyr1353His
XM_024451153.1:c.3979T>C XP_024306921.1:p.Tyr1327His
XM_024451154.1:c.3979T>C XP_024306922.1:p.Tyr1327His
XM_024451155.1:c.3979T>C XP_024306923.1:p.Tyr1327His
XM_024451156.1:c.4057T>C XP_024306924.1:p.Tyr1353His
XM_024451157.1:c.3502T>C XP_024306925.1:p.Tyr1168His
XM_024451158.1:c.4057T>C XP_024306926.1:p.Tyr1353His
NM_001379141.1:c.3979T>C NP_001366070.1:p.Tyr1327His
NM_001379142.1:c.3979T>C NP_001366071.1:p.Tyr1327His