Canonical Allele Identifier: CA2574036558

Gene: TSHB

Linked Data

• gnomAD v4: 1-115033349-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033349A>G , CM000663.2:g.115033349A>G	GRCh38
NC_000001.10:g.115575970A>G , CM000663.1:g.115575970A>G	GRCh37
NC_000001.9:g.115377493A>G	NCBI36
NG_015891.1:g.8556A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.-1-13A>G MANE Select	ENSP00000256592.1:n.-1-13A>G
ENST00000256592.2:c.-1-13A>G	ENSP00000256592.1:n.-1-13A>G
NM_000549.4:c.-1-13A>G	NP_000540.2:n.-1-13A>G
XM_011542065.1:c.-14A>G	XP_011540367.1:n.-14A>G
XM_011542065.2:c.-14A>G	XP_011540367.1:n.-14A>G
NM_000549.5:c.-1-13A>G MANE Select	NP_000540.2:n.-1-13A>G