Canonical Allele Identifier: CA2696606832

Gene: TSHB

Linked Data

• dbSNP Id: rs2101008940

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033783_115033784del , CM000663.2:g.115033783_115033784del	GRCh38
NC_000001.10:g.115576404_115576405del , CM000663.1:g.115576404_115576405del	GRCh37
NC_000001.9:g.115377927_115377928del	NCBI36
NG_015891.1:g.8990_8991del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.163-190_163-189del MANE Select	ENSP00000256592.1:n.163-190_163-189del
ENST00000256592.2:c.163-190_163-189del	ENSP00000256592.1:n.163-190_163-189del
ENST00000369517.1:c.163-190_163-189del	ENSP00000358530.1:n.163-190_163-189del
NM_000549.4:c.163-190_163-189del	NP_000540.2:n.163-190_163-189del
XM_011542065.1:c.163-190_163-189del	XP_011540367.1:n.163-190_163-189del
XM_011542065.2:c.163-190_163-189del	XP_011540367.1:n.163-190_163-189del
NM_000549.5:c.163-190_163-189del MANE Select	NP_000540.2:n.163-190_163-189del