Canonical Allele Identifier: CA1190425369
Gene: TSHB HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033842G= , CM000663.2:g.115033842G= GRCh38
NC_000001.10:g.115576463G= , CM000663.1:g.115576463G= GRCh37
NC_000001.9:g.115377986G= NCBI36
NG_015891.1:g.9049G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.163-131G= MANE Select ENSP00000256592.1:n.163-131G=
ENST00000256592.2:c.163-131G= ENSP00000256592.1:n.163-131G=
ENST00000369517.1:c.163-131G= ENSP00000358530.1:n.163-131G=
NM_000549.4:c.163-131G= NP_000540.2:n.163-131G=
XM_011542065.1:c.163-131G= XP_011540367.1:n.163-131G=
XM_011542065.2:c.163-131G= XP_011540367.1:n.163-131G=
NM_000549.5:c.163-131G= MANE Select NP_000540.2:n.163-131G=
Search 100 bp 5'
Search 100 bp 3'