Canonical Allele Identifier: CA341755152

Gene: TSHB

Linked Data

• MyVariant Identifiers: chr1:g.115576092G>A (hg19) ; chr1:g.115033471G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033471G>A , CM000663.2:g.115033471G>A	GRCh38
NC_000001.10:g.115576092G>A , CM000663.1:g.115576092G>A	GRCh37
NC_000001.9:g.115377615G>A	NCBI36
NG_015891.1:g.8678G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.109G>A MANE Select	ENSP00000256592.1:p.Ala37Thr
ENST00000256592.2:c.109G>A	ENSP00000256592.1:p.Ala37Thr
ENST00000369517.1:c.109G>A	ENSP00000358530.1:p.Ala37Thr
NM_000549.4:c.109G>A	NP_000540.2:p.Ala37Thr
XM_011542065.1:c.109G>A	XP_011540367.1:p.Ala37Thr
XM_011542065.2:c.109G>A	XP_011540367.1:p.Ala37Thr
NM_000549.5:c.109G>A MANE Select	NP_000540.2:p.Ala37Thr