Canonical Allele Identifier: CA29083511

Gene: TSHB

Linked Data

• dbSNP Id: rs926850907
• gnomAD v4: 1-115033457-A-G
• MyVariant Identifiers: chr1:g.115576078A>G (hg19) ; chr1:g.115033457A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.115033457A>G , CM000663.2:g.115033457A>G	GRCh38
NC_000001.10:g.115576078A>G , CM000663.1:g.115576078A>G	GRCh37
NC_000001.9:g.115377601A>G	NCBI36
NG_015891.1:g.8664A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256592.3:c.95A>G MANE Select	ENSP00000256592.1:p.Glu32Gly
ENST00000256592.2:c.95A>G	ENSP00000256592.1:p.Glu32Gly
ENST00000369517.1:c.95A>G	ENSP00000358530.1:p.Glu32Gly
NM_000549.4:c.95A>G	NP_000540.2:p.Glu32Gly
XM_011542065.1:c.95A>G	XP_011540367.1:p.Glu32Gly
XM_011542065.2:c.95A>G	XP_011540367.1:p.Glu32Gly
NM_000549.5:c.95A>G MANE Select	NP_000540.2:p.Glu32Gly