Canonical Allele Identifier: CA1190425372
Gene: TSHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033855T= , CM000663.2:g.115033855T= GRCh38
NC_000001.10:g.115576476T= , CM000663.1:g.115576476T= GRCh37
NC_000001.9:g.115377999T= NCBI36
NG_015891.1:g.9062T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.163-118T= MANE Select ENSP00000256592.1:n.163-118T=
ENST00000256592.2:c.163-118T= ENSP00000256592.1:n.163-118T=
ENST00000369517.1:c.163-118T= ENSP00000358530.1:n.163-118T=
NM_000549.4:c.163-118T= NP_000540.2:n.163-118T=
XM_011542065.1:c.163-118T= XP_011540367.1:n.163-118T=
XM_011542065.2:c.163-118T= XP_011540367.1:n.163-118T=
NM_000549.5:c.163-118T= MANE Select NP_000540.2:n.163-118T=
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