Canonical Allele Identifier: CA341754862
Gene: TSHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115576056A>C (hg19) chr1:g.115033435A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033435A>C , CM000663.2:g.115033435A>C GRCh38
NC_000001.10:g.115576056A>C , CM000663.1:g.115576056A>C GRCh37
NC_000001.9:g.115377579A>C NCBI36
NG_015891.1:g.8642A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.73A>C MANE Select ENSP00000256592.1:p.Thr25Pro
ENST00000256592.2:c.73A>C ENSP00000256592.1:p.Thr25Pro
ENST00000369517.1:c.73A>C ENSP00000358530.1:p.Thr25Pro
NM_000549.4:c.73A>C NP_000540.2:p.Thr25Pro
XM_011542065.1:c.73A>C XP_011540367.1:p.Thr25Pro
XM_011542065.2:c.73A>C XP_011540367.1:p.Thr25Pro
NM_000549.5:c.73A>C MANE Select NP_000540.2:p.Thr25Pro
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Search 100 bp 3'