Canonical Allele Identifier: CA885864987
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs1312729325
gnomAD v3: 1-115033304-G-C
gnomAD v4: 1-115033304-G-C
MyVariant Identifiers: chr1:g.115575925G>C (hg19) chr1:g.115033304G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033304G>C , CM000663.2:g.115033304G>C GRCh38
NC_000001.10:g.115575925G>C , CM000663.1:g.115575925G>C GRCh37
NC_000001.9:g.115377448G>C NCBI36
NG_015891.1:g.8511G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.-1-58G>C MANE Select ENSP00000256592.1:n.-1-58G>C
ENST00000256592.2:c.-1-58G>C ENSP00000256592.1:n.-1-58G>C
NM_000549.4:c.-1-58G>C NP_000540.2:n.-1-58G>C
XM_011542065.1:c.-59G>C XP_011540367.1:n.-59G>C
XM_011542065.2:c.-59G>C XP_011540367.1:n.-59G>C
NM_000549.5:c.-1-58G>C MANE Select NP_000540.2:n.-1-58G>C
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