Canonical Allele Identifier: CA1149110083

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033440G= , CM000663.2:g.115033440G=	GRCh38
NC_000001.10:g.115576061G= , CM000663.1:g.115576061G=	GRCh37
NC_000001.9:g.115377584G=	NCBI36
NG_015891.1:g.8647G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.78G= MANE Select	ENSP00000256592.1:p.Glu26=
ENST00000256592.2:c.78G=	ENSP00000256592.1:p.Glu26=
ENST00000369517.1:c.78G=	ENSP00000358530.1:p.Glu26=
NM_000549.4:c.78G=	NP_000540.2:p.Glu26=
XM_011542065.1:c.78G=	XP_011540367.1:p.Glu26=
XM_011542065.2:c.78G=	XP_011540367.1:p.Glu26=
NM_000549.5:c.78G= MANE Select	NP_000540.2:p.Glu26=