Canonical Allele Identifier: CA913047927
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs1674939386

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033466_115033467del , CM000663.2:g.115033466_115033467del GRCh38
NC_000001.10:g.115576087_115576088del , CM000663.1:g.115576087_115576088del GRCh37
NC_000001.9:g.115377610_115377611del NCBI36
NG_015891.1:g.8673_8674del

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.104_105del MANE Select ENSP00000256592.1:p.Glu35ValfsTer?
ENST00000256592.2:c.104_105del ENSP00000256592.1:p.Glu35ValfsTer?
ENST00000369517.1:c.104_105del ENSP00000358530.1:p.Glu35ValfsTer?
NM_000549.4:c.104_105del NP_000540.2:p.Glu35ValfsTer?
XM_011542065.1:c.104_105del XP_011540367.1:p.Glu35ValfsTer?
XM_011542065.2:c.104_105del XP_011540367.1:p.Glu35ValfsTer?
NM_000549.5:c.104_105del MANE Select NP_000540.2:p.Glu35ValfsTer?