Canonical Allele Identifier: CA1006029877
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs1570953469
gnomAD v3: 1-115033268-T-C
gnomAD v4: 1-115033268-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033268T>C , CM000663.2:g.115033268T>C GRCh38
NC_000001.10:g.115575889T>C , CM000663.1:g.115575889T>C GRCh37
NC_000001.9:g.115377412T>C NCBI36
NG_015891.1:g.8475T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.-1-94T>C MANE Select ENSP00000256592.1:n.-1-94T>C
ENST00000256592.2:c.-1-94T>C ENSP00000256592.1:n.-1-94T>C
NM_000549.4:c.-1-94T>C NP_000540.2:n.-1-94T>C
NM_000549.5:c.-1-94T>C MANE Select NP_000540.2:n.-1-94T>C
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