Canonical Allele Identifier: CA885865292

Gene: TSHB

Linked Data

• dbSNP Id: rs1314362676
• MyVariant Identifiers: chr1:g.115576153G>A (hg19) ; chr1:g.115033532G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033532G>A , CM000663.2:g.115033532G>A	GRCh38
NC_000001.10:g.115576153G>A , CM000663.1:g.115576153G>A	GRCh37
NC_000001.9:g.115377676G>A	NCBI36
NG_015891.1:g.8739G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.162+8G>A MANE Select	ENSP00000256592.1:n.162+8G>A
ENST00000256592.2:c.162+8G>A	ENSP00000256592.1:n.162+8G>A
ENST00000369517.1:c.162+8G>A	ENSP00000358530.1:n.162+8G>A
NM_000549.4:c.162+8G>A	NP_000540.2:n.162+8G>A
XM_011542065.1:c.162+8G>A	XP_011540367.1:n.162+8G>A
XM_011542065.2:c.162+8G>A	XP_011540367.1:n.162+8G>A
NM_000549.5:c.162+8G>A MANE Select	NP_000540.2:n.162+8G>A