Canonical Allele Identifier: CA29083554
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs267597940
MyVariant Identifiers: chr1:g.115576129G>A (hg19) chr1:g.115033508G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033508G>A , CM000663.2:g.115033508G>A GRCh38
NC_000001.10:g.115576129G>A , CM000663.1:g.115576129G>A GRCh37
NC_000001.9:g.115377652G>A NCBI36
NG_015891.1:g.8715G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.146G>A MANE Select ENSP00000256592.1:p.Gly49Glu
ENST00000256592.2:c.146G>A ENSP00000256592.1:p.Gly49Glu
ENST00000369517.1:c.146G>A ENSP00000358530.1:p.Gly49Glu
NM_000549.4:c.146G>A NP_000540.2:p.Gly49Glu
XM_011542065.1:c.146G>A XP_011540367.1:p.Gly49Glu
XM_011542065.2:c.146G>A XP_011540367.1:p.Gly49Glu
NM_000549.5:c.146G>A MANE Select NP_000540.2:p.Gly49Glu
Search 100 bp 5'
Search 100 bp 3'