Canonical Allele Identifier: CA2001397985
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1950045672

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113932441del , CM000673.2:g.113932441del GRCh38
NC_000011.9:g.113803163del , CM000673.1:g.113803163del GRCh37
NC_000011.8:g.113308373del NCBI36
NG_011483.1:g.32575del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260191.8:c.521del MANE Select ENSP00000260191.2:p.Lys174ArgfsTer10
ENST00000260191.7:c.521del ENSP00000260191.2:p.Lys174ArgfsTer10
ENST00000260191.6:c.521del ENSP00000260191.2:p.Lys174ArgfsTer10
ENST00000537778.5:c.488del ENSP00000443118.1:p.Lys163ArgfsTer10
ENST00000543092.1:c.307del
NM_006028.4:c.521del NP_006019.1:p.Lys174ArgfsTer10
XM_011543063.1:c.488del XP_011541365.1:p.Lys163ArgfsTer10
XM_011543064.1:c.320del XP_011541366.1:p.Lys107ArgfsTer10
XM_011543065.1:c.314del XP_011541367.1:p.Lys105ArgfsTer10
XM_011543066.1:c.488del XP_011541368.1:p.Lys163ArgfsTer10
NM_001363563.1:c.488del NP_001350492.1:p.Lys163ArgfsTer10
XM_017018552.2:c.314del XP_016874041.1:p.Lys105ArgfsTer10
XM_024448767.1:c.227del XP_024304535.1:p.Lys76ArgfsTer10
XR_001748034.2:n.772del
NM_001363563.2:c.488del NP_001350492.1:p.Lys163ArgfsTer10
NM_006028.5:c.521del MANE Select NP_006019.1:p.Lys174ArgfsTer10