Canonical Allele Identifier: CA885865351

Gene: TSHB

Linked Data

• dbSNP Id: rs1392964392
• MyVariant Identifiers: chr1:g.115576343del (hg19) ; chr1:g.115033722del (hg38)

Genomic Alleles

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

Transcript Alleles

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