Canonical Allele Identifier: CA419891300

Gene: TSHB

Linked Data

• MyVariant Identifiers: chr1:g.115576034A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033413A>G , CM000663.2:g.115033413A>G	GRCh38
NC_000001.10:g.115576034A>G , CM000663.1:g.115576034A>G	GRCh37
NC_000001.9:g.115377557A>G	NCBI36
NG_015891.1:g.8620A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.51A>G MANE Select	ENSP00000256592.1:p.Gln17=
ENST00000256592.2:c.51A>G	ENSP00000256592.1:p.Gln17=
ENST00000369517.1:c.51A>G	ENSP00000358530.1:p.Gln17=
NM_000549.4:c.51A>G	NP_000540.2:p.Gln17=
XM_011542065.1:c.51A>G	XP_011540367.1:p.Gln17=
XM_011542065.2:c.51A>G	XP_011540367.1:p.Gln17=
NM_000549.5:c.51A>G MANE Select	NP_000540.2:p.Gln17=