Canonical Allele Identifier: CA2647270315
Gene: TSHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033283del , CM000663.2:g.115033283del GRCh38
NC_000001.10:g.115575904del , CM000663.1:g.115575904del GRCh37
NC_000001.9:g.115377427del NCBI36
NG_015891.1:g.8490del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-79del MANE Select ENSP00000256592.1:n.-1-79del
ENST00000256592.2:c.-1-79del ENSP00000256592.1:n.-1-79del
NM_000549.4:c.-1-79del NP_000540.2:n.-1-79del
NM_000549.5:c.-1-79del MANE Select NP_000540.2:n.-1-79del