Canonical Allele Identifier: CA1145526590
Gene: TSHB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033293A= , CM000663.2:g.115033293A= GRCh38
NC_000001.10:g.115575914A= , CM000663.1:g.115575914A= GRCh37
NC_000001.9:g.115377437A= NCBI36
NG_015891.1:g.8500A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-69A= MANE Select ENSP00000256592.1:n.-1-69A=
ENST00000256592.2:c.-1-69A= ENSP00000256592.1:n.-1-69A=
NM_000549.4:c.-1-69A= NP_000540.2:n.-1-69A=
XM_011542065.2:c.-70A= XP_011540367.1:n.-70A=
NM_000549.5:c.-1-69A= MANE Select NP_000540.2:n.-1-69A=