Canonical Allele Identifier: CA2647270303
Gene: TSHB HGNC NCBI

Linked Data

gnomAD v4: 1-115033262-ATGCAT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033265_115033269del , CM000663.2:g.115033265_115033269del GRCh38
NC_000001.10:g.115575886_115575890del , CM000663.1:g.115575886_115575890del GRCh37
NC_000001.9:g.115377409_115377413del NCBI36
NG_015891.1:g.8472_8476del

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-97_-1-93del MANE Select ENSP00000256592.1:n.-1-97_-1-93del
ENST00000256592.2:c.-1-97_-1-93del ENSP00000256592.1:n.-1-97_-1-93del
NM_000549.4:c.-1-97_-1-93del NP_000540.2:n.-1-97_-1-93del
NM_000549.5:c.-1-97_-1-93del MANE Select NP_000540.2:n.-1-97_-1-93del
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