Canonical Allele Identifier: CA341755403
Gene: TSHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033516A>C , CM000663.2:g.115033516A>C GRCh38
NC_000001.10:g.115576137A>C , CM000663.1:g.115576137A>C GRCh37
NC_000001.9:g.115377660A>C NCBI36
NG_015891.1:g.8723A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.154A>C MANE Select ENSP00000256592.1:p.Met52Leu
ENST00000256592.2:c.154A>C ENSP00000256592.1:p.Met52Leu
ENST00000369517.1:c.154A>C ENSP00000358530.1:p.Met52Leu
NM_000549.4:c.154A>C NP_000540.2:p.Met52Leu
XM_011542065.1:c.154A>C XP_011540367.1:p.Met52Leu
XM_011542065.2:c.154A>C XP_011540367.1:p.Met52Leu
NM_000549.5:c.154A>C MANE Select NP_000540.2:p.Met52Leu