Canonical Allele Identifier: CA1190425166

Gene: TSHB

Linked Data

• dbSNP Id: rs1674934236

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033291A>T , CM000663.2:g.115033291A>T	GRCh38
NC_000001.10:g.115575912A>T , CM000663.1:g.115575912A>T	GRCh37
NC_000001.9:g.115377435A>T	NCBI36
NG_015891.1:g.8498A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.-1-71A>T MANE Select	ENSP00000256592.1:n.-1-71A>T
ENST00000256592.2:c.-1-71A>T	ENSP00000256592.1:n.-1-71A>T
NM_000549.4:c.-1-71A>T	NP_000540.2:n.-1-71A>T
XM_011542065.2:c.-72A>T	XP_011540367.1:n.-72A>T
NM_000549.5:c.-1-71A>T MANE Select	NP_000540.2:n.-1-71A>T