Canonical Allele Identifier: CA2647270496
Gene: TSHB HGNC NCBI

Linked Data

gnomAD v4: 1-115033892-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033894del , CM000663.2:g.115033894del GRCh38
NC_000001.10:g.115576515del , CM000663.1:g.115576515del GRCh37
NC_000001.9:g.115378038del NCBI36
NG_015891.1:g.9101del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.163-79del MANE Select ENSP00000256592.1:n.163-79del
ENST00000256592.2:c.163-79del ENSP00000256592.1:n.163-79del
ENST00000369517.1:c.163-79del ENSP00000358530.1:n.163-79del
NM_000549.4:c.163-79del NP_000540.2:n.163-79del
XM_011542065.1:c.163-79del XP_011540367.1:n.163-79del
XM_011542065.2:c.163-79del XP_011540367.1:n.163-79del
NM_000549.5:c.163-79del MANE Select NP_000540.2:n.163-79del
Search 100 bp 5'
Search 100 bp 3'