Canonical Allele Identifier: CA419891423

Gene: TSHB

Linked Data

• MyVariant Identifiers: chr1:g.115576118C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033497C>G , CM000663.2:g.115033497C>G	GRCh38
NC_000001.10:g.115576118C>G , CM000663.1:g.115576118C>G	GRCh37
NC_000001.9:g.115377641C>G	NCBI36
NG_015891.1:g.8704C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.135C>G MANE Select	ENSP00000256592.1:p.Thr45=
ENST00000256592.2:c.135C>G	ENSP00000256592.1:p.Thr45=
ENST00000369517.1:c.135C>G	ENSP00000358530.1:p.Thr45=
NM_000549.4:c.135C>G	NP_000540.2:p.Thr45=
XM_011542065.1:c.135C>G	XP_011540367.1:p.Thr45=
XM_011542065.2:c.135C>G	XP_011540367.1:p.Thr45=
NM_000549.5:c.135C>G MANE Select	NP_000540.2:p.Thr45=