Canonical Allele Identifier: CA2647270307
Gene: TSHB HGNC NCBI

Linked Data

gnomAD v4: 1-115033269-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033269G>T , CM000663.2:g.115033269G>T GRCh38
NC_000001.10:g.115575890G>T , CM000663.1:g.115575890G>T GRCh37
NC_000001.9:g.115377413G>T NCBI36
NG_015891.1:g.8476G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.-1-93G>T MANE Select ENSP00000256592.1:n.-1-93G>T
ENST00000256592.2:c.-1-93G>T ENSP00000256592.1:n.-1-93G>T
NM_000549.4:c.-1-93G>T NP_000540.2:n.-1-93G>T
NM_000549.5:c.-1-93G>T MANE Select NP_000540.2:n.-1-93G>T
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Search 100 bp 3'