Canonical Allele Identifier: CA2574036548

Gene: TSHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033265C>T , CM000663.2:g.115033265C>T	GRCh38
NC_000001.10:g.115575886C>T , CM000663.1:g.115575886C>T	GRCh37
NC_000001.9:g.115377409C>T	NCBI36
NG_015891.1:g.8472C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.-1-97C>T MANE Select	ENSP00000256592.1:n.-1-97C>T
ENST00000256592.2:c.-1-97C>T	ENSP00000256592.1:n.-1-97C>T
NM_000549.4:c.-1-97C>T	NP_000540.2:n.-1-97C>T
NM_000549.5:c.-1-97C>T MANE Select	NP_000540.2:n.-1-97C>T