Canonical Allele Identifier: CA1190425173
Gene: TSHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033335G= , CM000663.2:g.115033335G= GRCh38
NC_000001.10:g.115575956G= , CM000663.1:g.115575956G= GRCh37
NC_000001.9:g.115377479G= NCBI36
NG_015891.1:g.8542G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-27G= MANE Select ENSP00000256592.1:n.-1-27G=
ENST00000256592.2:c.-1-27G= ENSP00000256592.1:n.-1-27G=
NM_000549.4:c.-1-27G= NP_000540.2:n.-1-27G=
XM_011542065.1:c.-28G= XP_011540367.1:n.-28G=
XM_011542065.2:c.-28G= XP_011540367.1:n.-28G=
NM_000549.5:c.-1-27G= MANE Select NP_000540.2:n.-1-27G=
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