Canonical Allele Identifier: CA1190425237
Gene: TSHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033521A= , CM000663.2:g.115033521A= GRCh38
NC_000001.10:g.115576142A= , CM000663.1:g.115576142A= GRCh37
NC_000001.9:g.115377665A= NCBI36
NG_015891.1:g.8728A=

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.159A= MANE Select ENSP00000256592.1:p.Thr53=
ENST00000256592.2:c.159A= ENSP00000256592.1:p.Thr53=
ENST00000369517.1:c.159A= ENSP00000358530.1:p.Thr53=
NM_000549.4:c.159A= NP_000540.2:p.Thr53=
XM_011542065.1:c.159A= XP_011540367.1:p.Thr53=
XM_011542065.2:c.159A= XP_011540367.1:p.Thr53=
NM_000549.5:c.159A= MANE Select NP_000540.2:p.Thr53=