Canonical Allele Identifier: CA1190425152
Gene: TSHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033263T= , CM000663.2:g.115033263T= GRCh38
NC_000001.10:g.115575884T= , CM000663.1:g.115575884T= GRCh37
NC_000001.9:g.115377407T= NCBI36
NG_015891.1:g.8470T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-99T= MANE Select ENSP00000256592.1:n.-1-99T=
ENST00000256592.2:c.-1-99T= ENSP00000256592.1:n.-1-99T=
NM_000549.4:c.-1-99T= NP_000540.2:n.-1-99T=
NM_000549.5:c.-1-99T= MANE Select NP_000540.2:n.-1-99T=