Canonical Allele Identifier: CA2647270316
Gene: TSHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033283G>T , CM000663.2:g.115033283G>T GRCh38
NC_000001.10:g.115575904G>T , CM000663.1:g.115575904G>T GRCh37
NC_000001.9:g.115377427G>T NCBI36
NG_015891.1:g.8490G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-79G>T MANE Select ENSP00000256592.1:n.-1-79G>T
ENST00000256592.2:c.-1-79G>T ENSP00000256592.1:n.-1-79G>T
NM_000549.4:c.-1-79G>T NP_000540.2:n.-1-79G>T
NM_000549.5:c.-1-79G>T MANE Select NP_000540.2:n.-1-79G>T