Canonical Allele Identifier: CA1145125384

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033555T= , CM000663.2:g.115033555T=	GRCh38
NC_000001.10:g.115576176T= , CM000663.1:g.115576176T=	GRCh37
NC_000001.9:g.115377699T=	NCBI36
NG_015891.1:g.8762T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.162+31T= MANE Select	ENSP00000256592.1:n.162+31T=
ENST00000256592.2:c.162+31T=	ENSP00000256592.1:n.162+31T=
ENST00000369517.1:c.162+31T=	ENSP00000358530.1:n.162+31T=
NM_000549.4:c.162+31T=	NP_000540.2:n.162+31T=
XM_011542065.1:c.162+31T=	XP_011540367.1:n.162+31T=
XM_011542065.2:c.162+31T=	XP_011540367.1:n.162+31T=
NM_000549.5:c.162+31T= MANE Select	NP_000540.2:n.162+31T=