Canonical Allele Identifier: CA2647270321

Gene: TSHB

Linked Data

• gnomAD v4: 1-115033300-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033300C>A , CM000663.2:g.115033300C>A	GRCh38
NC_000001.10:g.115575921C>A , CM000663.1:g.115575921C>A	GRCh37
NC_000001.9:g.115377444C>A	NCBI36
NG_015891.1:g.8507C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.-1-62C>A MANE Select	ENSP00000256592.1:n.-1-62C>A
ENST00000256592.2:c.-1-62C>A	ENSP00000256592.1:n.-1-62C>A
NM_000549.4:c.-1-62C>A	NP_000540.2:n.-1-62C>A
XM_011542065.2:c.-63C>A	XP_011540367.1:n.-63C>A
NM_000549.5:c.-1-62C>A MANE Select	NP_000540.2:n.-1-62C>A