Canonical Allele Identifier: CA1022526
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs768525725

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033447A>G , CM000663.2:g.115033447A>G GRCh38
NC_000001.10:g.115576068A>G , CM000663.1:g.115576068A>G GRCh37
NC_000001.9:g.115377591A>G NCBI36
NG_015891.1:g.8654A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.85A>G MANE Select ENSP00000256592.1:p.Met29Val
ENST00000256592.2:c.85A>G ENSP00000256592.1:p.Met29Val
ENST00000369517.1:c.85A>G ENSP00000358530.1:p.Met29Val
NM_000549.4:c.85A>G NP_000540.2:p.Met29Val
XM_011542065.1:c.85A>G XP_011540367.1:p.Met29Val
XM_011542065.2:c.85A>G XP_011540367.1:p.Met29Val
NM_000549.5:c.85A>G MANE Select NP_000540.2:p.Met29Val