Canonical Allele Identifier: CA29083450
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs868162505
gnomAD v4: 1-115033409-G-A
MyVariant Identifiers: chr1:g.115576030G>A (hg19) chr1:g.115033409G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033409G>A , CM000663.2:g.115033409G>A GRCh38
NC_000001.10:g.115576030G>A , CM000663.1:g.115576030G>A GRCh37
NC_000001.9:g.115377553G>A NCBI36
NG_015891.1:g.8616G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.47G>A MANE Select ENSP00000256592.1:p.Gly16Glu
ENST00000256592.2:c.47G>A ENSP00000256592.1:p.Gly16Glu
ENST00000369517.1:c.47G>A ENSP00000358530.1:p.Gly16Glu
NM_000549.4:c.47G>A NP_000540.2:p.Gly16Glu
XM_011542065.1:c.47G>A XP_011540367.1:p.Gly16Glu
XM_011542065.2:c.47G>A XP_011540367.1:p.Gly16Glu
NM_000549.5:c.47G>A MANE Select NP_000540.2:p.Gly16Glu
Search 100 bp 5'
Search 100 bp 3'