Canonical Allele Identifier: CA341754894

Gene: TSHB

Linked Data

• MyVariant Identifiers: chr1:g.115576060A>T (hg19) ; chr1:g.115033439A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033439A>T , CM000663.2:g.115033439A>T	GRCh38
NC_000001.10:g.115576060A>T , CM000663.1:g.115576060A>T	GRCh37
NC_000001.9:g.115377583A>T	NCBI36
NG_015891.1:g.8646A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.77A>T MANE Select	ENSP00000256592.1:p.Glu26Val
ENST00000256592.2:c.77A>T	ENSP00000256592.1:p.Glu26Val
ENST00000369517.1:c.77A>T	ENSP00000358530.1:p.Glu26Val
NM_000549.4:c.77A>T	NP_000540.2:p.Glu26Val
XM_011542065.1:c.77A>T	XP_011540367.1:p.Glu26Val
XM_011542065.2:c.77A>T	XP_011540367.1:p.Glu26Val
NM_000549.5:c.77A>T MANE Select	NP_000540.2:p.Glu26Val