Canonical Allele Identifier: CA1190425163
Gene: TSHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033280G= , CM000663.2:g.115033280G= GRCh38
NC_000001.10:g.115575901G= , CM000663.1:g.115575901G= GRCh37
NC_000001.9:g.115377424G= NCBI36
NG_015891.1:g.8487G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-82G= MANE Select ENSP00000256592.1:n.-1-82G=
ENST00000256592.2:c.-1-82G= ENSP00000256592.1:n.-1-82G=
NM_000549.4:c.-1-82G= NP_000540.2:n.-1-82G=
NM_000549.5:c.-1-82G= MANE Select NP_000540.2:n.-1-82G=
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