Canonical Allele Identifier: CA29083358
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs1049422560
gnomAD v4: 1-115033283-G-A
MyVariant Identifiers: chr1:g.115575904G>A (hg19) chr1:g.115033283G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033283G>A , CM000663.2:g.115033283G>A GRCh38
NC_000001.10:g.115575904G>A , CM000663.1:g.115575904G>A GRCh37
NC_000001.9:g.115377427G>A NCBI36
NG_015891.1:g.8490G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.-1-79G>A MANE Select ENSP00000256592.1:n.-1-79G>A
ENST00000256592.2:c.-1-79G>A ENSP00000256592.1:n.-1-79G>A
NM_000549.4:c.-1-79G>A NP_000540.2:n.-1-79G>A
NM_000549.5:c.-1-79G>A MANE Select NP_000540.2:n.-1-79G>A
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