Canonical Allele Identifier: CA1148289212

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033428T= , CM000663.2:g.115033428T=	GRCh38
NC_000001.10:g.115576049T= , CM000663.1:g.115576049T=	GRCh37
NC_000001.9:g.115377572T=	NCBI36
NG_015891.1:g.8635T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.66T= MANE Select	ENSP00000256592.1:p.Cys22=
ENST00000256592.2:c.66T=	ENSP00000256592.1:p.Cys22=
ENST00000369517.1:c.66T=	ENSP00000358530.1:p.Cys22=
NM_000549.4:c.66T=	NP_000540.2:p.Cys22=
XM_011542065.1:c.66T=	XP_011540367.1:p.Cys22=
XM_011542065.2:c.66T=	XP_011540367.1:p.Cys22=
NM_000549.5:c.66T= MANE Select	NP_000540.2:p.Cys22=