Canonical Allele Identifier: CA1190425168
Gene: TSHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033295T= , CM000663.2:g.115033295T= GRCh38
NC_000001.10:g.115575916T= , CM000663.1:g.115575916T= GRCh37
NC_000001.9:g.115377439T= NCBI36
NG_015891.1:g.8502T=

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.-1-67T= MANE Select ENSP00000256592.1:n.-1-67T=
ENST00000256592.2:c.-1-67T= ENSP00000256592.1:n.-1-67T=
NM_000549.4:c.-1-67T= NP_000540.2:n.-1-67T=
XM_011542065.2:c.-68T= XP_011540367.1:n.-68T=
NM_000549.5:c.-1-67T= MANE Select NP_000540.2:n.-1-67T=