Canonical Allele Identifier: CA2647270314
Gene: TSHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033279T>G , CM000663.2:g.115033279T>G GRCh38
NC_000001.10:g.115575900T>G , CM000663.1:g.115575900T>G GRCh37
NC_000001.9:g.115377423T>G NCBI36
NG_015891.1:g.8486T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-83T>G MANE Select ENSP00000256592.1:n.-1-83T>G
ENST00000256592.2:c.-1-83T>G ENSP00000256592.1:n.-1-83T>G
NM_000549.4:c.-1-83T>G NP_000540.2:n.-1-83T>G
NM_000549.5:c.-1-83T>G MANE Select NP_000540.2:n.-1-83T>G