Canonical Allele Identifier: CA885865368
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs1489673493
gnomAD v4: 1-115033770-A-C
MyVariant Identifiers: chr1:g.115576391A>C (hg19) chr1:g.115033770A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033770A>C , CM000663.2:g.115033770A>C GRCh38
NC_000001.10:g.115576391A>C , CM000663.1:g.115576391A>C GRCh37
NC_000001.9:g.115377914A>C NCBI36
NG_015891.1:g.8977A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.163-203A>C MANE Select ENSP00000256592.1:n.163-203A>C
ENST00000256592.2:c.163-203A>C ENSP00000256592.1:n.163-203A>C
ENST00000369517.1:c.163-203A>C ENSP00000358530.1:n.163-203A>C
NM_000549.4:c.163-203A>C NP_000540.2:n.163-203A>C
XM_011542065.1:c.163-203A>C XP_011540367.1:n.163-203A>C
XM_011542065.2:c.163-203A>C XP_011540367.1:n.163-203A>C
NM_000549.5:c.163-203A>C MANE Select NP_000540.2:n.163-203A>C
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