Canonical Allele Identifier: CA2647270308
Gene: TSHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033270G>A , CM000663.2:g.115033270G>A GRCh38
NC_000001.10:g.115575891G>A , CM000663.1:g.115575891G>A GRCh37
NC_000001.9:g.115377414G>A NCBI36
NG_015891.1:g.8477G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-92G>A MANE Select ENSP00000256592.1:n.-1-92G>A
ENST00000256592.2:c.-1-92G>A ENSP00000256592.1:n.-1-92G>A
NM_000549.4:c.-1-92G>A NP_000540.2:n.-1-92G>A
NM_000549.5:c.-1-92G>A MANE Select NP_000540.2:n.-1-92G>A