Canonical Allele Identifier: CA2566239771

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033345T>G , CM000663.2:g.115033345T>G	GRCh38
NC_000001.10:g.115575966T>G , CM000663.1:g.115575966T>G	GRCh37
NC_000001.9:g.115377489T>G	NCBI36
NG_015891.1:g.8552T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.-1-17T>G MANE Select	ENSP00000256592.1:n.-1-17T>G
ENST00000256592.2:c.-1-17T>G	ENSP00000256592.1:n.-1-17T>G
NM_000549.4:c.-1-17T>G	NP_000540.2:n.-1-17T>G
XM_011542065.1:c.-18T>G	XP_011540367.1:n.-18T>G
XM_011542065.2:c.-18T>G	XP_011540367.1:n.-18T>G
NM_000549.5:c.-1-17T>G MANE Select	NP_000540.2:n.-1-17T>G