Canonical Allele Identifier: CA2745142335
Gene: TSHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033287G>C , CM000663.2:g.115033287G>C GRCh38
NC_000001.10:g.115575908G>C , CM000663.1:g.115575908G>C GRCh37
NC_000001.9:g.115377431G>C NCBI36
NG_015891.1:g.8494G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-75G>C MANE Select ENSP00000256592.1:n.-1-75G>C
ENST00000256592.2:c.-1-75G>C ENSP00000256592.1:n.-1-75G>C
NM_000549.4:c.-1-75G>C NP_000540.2:n.-1-75G>C
XM_011542065.2:c.-76G>C XP_011540367.1:n.-76G>C
NM_000549.5:c.-1-75G>C MANE Select NP_000540.2:n.-1-75G>C