Canonical Allele Identifier: CA2647270343
Gene: TSHB HGNC NCBI

Linked Data

gnomAD v4: 1-115033383-GTCC-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033384_115033386del , CM000663.2:g.115033384_115033386del GRCh38
NC_000001.10:g.115576005_115576007del , CM000663.1:g.115576005_115576007del GRCh37
NC_000001.9:g.115377528_115377530del NCBI36
NG_015891.1:g.8591_8593del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.22_24del MANE Select ENSP00000256592.1:p.Ser8del
ENST00000256592.2:c.22_24del ENSP00000256592.1:p.Ser8del
ENST00000369517.1:c.22_24del ENSP00000358530.1:p.Ser8del
NM_000549.4:c.22_24del NP_000540.2:p.Ser8del
XM_011542065.1:c.22_24del XP_011540367.1:p.Ser8del
XM_011542065.2:c.22_24del XP_011540367.1:p.Ser8del
NM_000549.5:c.22_24del MANE Select NP_000540.2:p.Ser8del
Search 100 bp 5'
Search 100 bp 3'