Canonical Allele Identifier: CA2647270264
Gene: TSHB HGNC NCBI

Linked Data

gnomAD v4: 1-115033197-C-CT
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033203dup , CM000663.2:g.115033203dup GRCh38
NC_000001.10:g.115575824dup , CM000663.1:g.115575824dup GRCh37
NC_000001.9:g.115377347dup NCBI36
NG_015891.1:g.8410dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-159dup MANE Select ENSP00000256592.1:n.-1-159dup
ENST00000256592.2:c.-1-159dup ENSP00000256592.1:n.-1-159dup
NM_000549.4:c.-1-159dup NP_000540.2:n.-1-159dup
NM_000549.5:c.-1-159dup MANE Select NP_000540.2:n.-1-159dup
Search 100 bp 5'
Search 100 bp 3'