Canonical Allele Identifier: CA341754821
Gene: TSHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115576050A>C (hg19) chr1:g.115033429A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033429A>C , CM000663.2:g.115033429A>C GRCh38
NC_000001.10:g.115576050A>C , CM000663.1:g.115576050A>C GRCh37
NC_000001.9:g.115377573A>C NCBI36
NG_015891.1:g.8636A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.67A>C MANE Select ENSP00000256592.1:p.Ile23Leu
ENST00000256592.2:c.67A>C ENSP00000256592.1:p.Ile23Leu
ENST00000369517.1:c.67A>C ENSP00000358530.1:p.Ile23Leu
NM_000549.4:c.67A>C NP_000540.2:p.Ile23Leu
XM_011542065.1:c.67A>C XP_011540367.1:p.Ile23Leu
XM_011542065.2:c.67A>C XP_011540367.1:p.Ile23Leu
NM_000549.5:c.67A>C MANE Select NP_000540.2:p.Ile23Leu
Search 100 bp 5'
Search 100 bp 3'