Canonical Allele Identifier: CA2647270438

Gene: TSHB

Linked Data

• gnomAD v4: 1-115033784-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033784G>C , CM000663.2:g.115033784G>C	GRCh38
NC_000001.10:g.115576405G>C , CM000663.1:g.115576405G>C	GRCh37
NC_000001.9:g.115377928G>C	NCBI36
NG_015891.1:g.8991G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.163-189G>C MANE Select	ENSP00000256592.1:n.163-189G>C
ENST00000256592.2:c.163-189G>C	ENSP00000256592.1:n.163-189G>C
ENST00000369517.1:c.163-189G>C	ENSP00000358530.1:n.163-189G>C
NM_000549.4:c.163-189G>C	NP_000540.2:n.163-189G>C
XM_011542065.1:c.163-189G>C	XP_011540367.1:n.163-189G>C
XM_011542065.2:c.163-189G>C	XP_011540367.1:n.163-189G>C
NM_000549.5:c.163-189G>C MANE Select	NP_000540.2:n.163-189G>C