Canonical Allele Identifier: CA1190425362
Gene: TSHB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033817C= , CM000663.2:g.115033817C= GRCh38
NC_000001.10:g.115576438C= , CM000663.1:g.115576438C= GRCh37
NC_000001.9:g.115377961C= NCBI36
NG_015891.1:g.9024C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.163-156C= MANE Select ENSP00000256592.1:n.163-156C=
ENST00000256592.2:c.163-156C= ENSP00000256592.1:n.163-156C=
ENST00000369517.1:c.163-156C= ENSP00000358530.1:n.163-156C=
NM_000549.4:c.163-156C= NP_000540.2:n.163-156C=
XM_011542065.1:c.163-156C= XP_011540367.1:n.163-156C=
XM_011542065.2:c.163-156C= XP_011540367.1:n.163-156C=
NM_000549.5:c.163-156C= MANE Select NP_000540.2:n.163-156C=
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