Canonical Allele Identifier: CA341754975
Gene: TSHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033450C>T , CM000663.2:g.115033450C>T GRCh38
NC_000001.10:g.115576071C>T , CM000663.1:g.115576071C>T GRCh37
NC_000001.9:g.115377594C>T NCBI36
NG_015891.1:g.8657C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.88C>T MANE Select ENSP00000256592.1:p.His30Tyr
ENST00000256592.2:c.88C>T ENSP00000256592.1:p.His30Tyr
ENST00000369517.1:c.88C>T ENSP00000358530.1:p.His30Tyr
NM_000549.4:c.88C>T NP_000540.2:p.His30Tyr
XM_011542065.1:c.88C>T XP_011540367.1:p.His30Tyr
XM_011542065.2:c.88C>T XP_011540367.1:p.His30Tyr
NM_000549.5:c.88C>T MANE Select NP_000540.2:p.His30Tyr