Canonical Allele Identifier: CA1190425171

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033321G= , CM000663.2:g.115033321G=	GRCh38
NC_000001.10:g.115575942G= , CM000663.1:g.115575942G=	GRCh37
NC_000001.9:g.115377465G=	NCBI36
NG_015891.1:g.8528G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.-1-41G= MANE Select	ENSP00000256592.1:n.-1-41G=
ENST00000256592.2:c.-1-41G=	ENSP00000256592.1:n.-1-41G=
NM_000549.4:c.-1-41G=	NP_000540.2:n.-1-41G=
XM_011542065.1:c.-42G=	XP_011540367.1:n.-42G=
XM_011542065.2:c.-42G=	XP_011540367.1:n.-42G=
NM_000549.5:c.-1-41G= MANE Select	NP_000540.2:n.-1-41G=