Canonical Allele Identifier: CA1190425236
Gene: TSHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033518G= , CM000663.2:g.115033518G= GRCh38
NC_000001.10:g.115576139G= , CM000663.1:g.115576139G= GRCh37
NC_000001.9:g.115377662G= NCBI36
NG_015891.1:g.8725G=

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.156G= MANE Select ENSP00000256592.1:p.Met52=
ENST00000256592.2:c.156G= ENSP00000256592.1:p.Met52=
ENST00000369517.1:c.156G= ENSP00000358530.1:p.Met52=
NM_000549.4:c.156G= NP_000540.2:p.Met52=
XM_011542065.1:c.156G= XP_011540367.1:p.Met52=
XM_011542065.2:c.156G= XP_011540367.1:p.Met52=
NM_000549.5:c.156G= MANE Select NP_000540.2:p.Met52=