Canonical Allele Identifier: CA2520170337
Gene: TSHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033567del , CM000663.2:g.115033567del GRCh38
NC_000001.10:g.115576188del , CM000663.1:g.115576188del GRCh37
NC_000001.9:g.115377711del NCBI36
NG_015891.1:g.8774del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.162+43del MANE Select ENSP00000256592.1:n.162+43del
ENST00000256592.2:c.162+43del ENSP00000256592.1:n.162+43del
ENST00000369517.1:c.162+43del ENSP00000358530.1:n.162+43del
NM_000549.4:c.162+43del NP_000540.2:n.162+43del
XM_011542065.1:c.162+43del XP_011540367.1:n.162+43del
XM_011542065.2:c.162+43del XP_011540367.1:n.162+43del
NM_000549.5:c.162+43del MANE Select NP_000540.2:n.162+43del
Search 100 bp 5'
Search 100 bp 3'