Canonical Allele Identifier: CA1147743945
Gene: TSHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033261T= , CM000663.2:g.115033261T= GRCh38
NC_000001.10:g.115575882T= , CM000663.1:g.115575882T= GRCh37
NC_000001.9:g.115377405T= NCBI36
NG_015891.1:g.8468T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-101T= MANE Select ENSP00000256592.1:n.-1-101T=
ENST00000256592.2:c.-1-101T= ENSP00000256592.1:n.-1-101T=
NM_000549.4:c.-1-101T= NP_000540.2:n.-1-101T=
NM_000549.5:c.-1-101T= MANE Select NP_000540.2:n.-1-101T=
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