Canonical Allele Identifier: CA1190425206

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033431T= , CM000663.2:g.115033431T=	GRCh38
NC_000001.10:g.115576052T= , CM000663.1:g.115576052T=	GRCh37
NC_000001.9:g.115377575T=	NCBI36
NG_015891.1:g.8638T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.69T= MANE Select	ENSP00000256592.1:p.Ile23=
ENST00000256592.2:c.69T=	ENSP00000256592.1:p.Ile23=
ENST00000369517.1:c.69T=	ENSP00000358530.1:p.Ile23=
NM_000549.4:c.69T=	NP_000540.2:p.Ile23=
XM_011542065.1:c.69T=	XP_011540367.1:p.Ile23=
XM_011542065.2:c.69T=	XP_011540367.1:p.Ile23=
NM_000549.5:c.69T= MANE Select	NP_000540.2:p.Ile23=