Canonical Allele Identifier: CA419891320
Gene: TSHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115576058T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033437T>G , CM000663.2:g.115033437T>G GRCh38
NC_000001.10:g.115576058T>G , CM000663.1:g.115576058T>G GRCh37
NC_000001.9:g.115377581T>G NCBI36
NG_015891.1:g.8644T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.75T>G MANE Select ENSP00000256592.1:p.Thr25=
ENST00000256592.2:c.75T>G ENSP00000256592.1:p.Thr25=
ENST00000369517.1:c.75T>G ENSP00000358530.1:p.Thr25=
NM_000549.4:c.75T>G NP_000540.2:p.Thr25=
XM_011542065.1:c.75T>G XP_011540367.1:p.Thr25=
XM_011542065.2:c.75T>G XP_011540367.1:p.Thr25=
NM_000549.5:c.75T>G MANE Select NP_000540.2:p.Thr25=