Canonical Allele Identifier: CA885865349

Gene: TSHB

Linked Data

• dbSNP Id: rs1303008963
• MyVariant Identifiers: chr1:g.115576342_115576343del (hg19) ; chr1:g.115033721_115033722del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033722_115033723del , CM000663.2:g.115033722_115033723del	GRCh38
NC_000001.10:g.115576343_115576344del , CM000663.1:g.115576343_115576344del	GRCh37
NC_000001.9:g.115377866_115377867del	NCBI36
NG_015891.1:g.8929_8930del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.162+198_162+199del MANE Select	ENSP00000256592.1:n.162+198_162+199del
ENST00000256592.2:c.162+198_162+199del	ENSP00000256592.1:n.162+198_162+199del
ENST00000369517.1:c.162+198_162+199del	ENSP00000358530.1:n.162+198_162+199del
NM_000549.4:c.162+198_162+199del	NP_000540.2:n.162+198_162+199del
XM_011542065.1:c.162+198_162+199del	XP_011540367.1:n.162+198_162+199del
XM_011542065.2:c.162+198_162+199del	XP_011540367.1:n.162+198_162+199del
NM_000549.5:c.162+198_162+199del MANE Select	NP_000540.2:n.162+198_162+199del