Canonical Allele Identifier: CA1006029881
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs1557870085
gnomAD v3: 1-115033280-G-C
gnomAD v4: 1-115033280-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033280G>C , CM000663.2:g.115033280G>C GRCh38
NC_000001.10:g.115575901G>C , CM000663.1:g.115575901G>C GRCh37
NC_000001.9:g.115377424G>C NCBI36
NG_015891.1:g.8487G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-82G>C MANE Select ENSP00000256592.1:n.-1-82G>C
ENST00000256592.2:c.-1-82G>C ENSP00000256592.1:n.-1-82G>C
NM_000549.4:c.-1-82G>C NP_000540.2:n.-1-82G>C
NM_000549.5:c.-1-82G>C MANE Select NP_000540.2:n.-1-82G>C
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