Canonical Allele Identifier: CA2647270382
Gene: TSHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033610A>T , CM000663.2:g.115033610A>T GRCh38
NC_000001.10:g.115576231A>T , CM000663.1:g.115576231A>T GRCh37
NC_000001.9:g.115377754A>T NCBI36
NG_015891.1:g.8817A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.162+86A>T MANE Select ENSP00000256592.1:n.162+86A>T
ENST00000256592.2:c.162+86A>T ENSP00000256592.1:n.162+86A>T
ENST00000369517.1:c.162+86A>T ENSP00000358530.1:n.162+86A>T
NM_000549.4:c.162+86A>T NP_000540.2:n.162+86A>T
XM_011542065.1:c.162+86A>T XP_011540367.1:n.162+86A>T
XM_011542065.2:c.162+86A>T XP_011540367.1:n.162+86A>T
NM_000549.5:c.162+86A>T MANE Select NP_000540.2:n.162+86A>T