Canonical Allele Identifier: CA1190425158

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033274G= , CM000663.2:g.115033274G=	GRCh38
NC_000001.10:g.115575895G= , CM000663.1:g.115575895G=	GRCh37
NC_000001.9:g.115377418G=	NCBI36
NG_015891.1:g.8481G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.-1-88G= MANE Select	ENSP00000256592.1:n.-1-88G=
ENST00000256592.2:c.-1-88G=	ENSP00000256592.1:n.-1-88G=
NM_000549.4:c.-1-88G=	NP_000540.2:n.-1-88G=
NM_000549.5:c.-1-88G= MANE Select	NP_000540.2:n.-1-88G=