Canonical Allele Identifier: CA2647270476

Gene: TSHB

Linked Data

• gnomAD v4: 1-115033850-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033850G>T , CM000663.2:g.115033850G>T	GRCh38
NC_000001.10:g.115576471G>T , CM000663.1:g.115576471G>T	GRCh37
NC_000001.9:g.115377994G>T	NCBI36
NG_015891.1:g.9057G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.163-123G>T MANE Select	ENSP00000256592.1:n.163-123G>T
ENST00000256592.2:c.163-123G>T	ENSP00000256592.1:n.163-123G>T
ENST00000369517.1:c.163-123G>T	ENSP00000358530.1:n.163-123G>T
NM_000549.4:c.163-123G>T	NP_000540.2:n.163-123G>T
XM_011542065.1:c.163-123G>T	XP_011540367.1:n.163-123G>T
XM_011542065.2:c.163-123G>T	XP_011540367.1:n.163-123G>T
NM_000549.5:c.163-123G>T MANE Select	NP_000540.2:n.163-123G>T