Canonical Allele Identifier: CA2647270324
Gene: TSHB HGNC NCBI

Linked Data

gnomAD v4: 1-115033303-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033303G>A , CM000663.2:g.115033303G>A GRCh38
NC_000001.10:g.115575924G>A , CM000663.1:g.115575924G>A GRCh37
NC_000001.9:g.115377447G>A NCBI36
NG_015891.1:g.8510G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.-1-59G>A MANE Select ENSP00000256592.1:n.-1-59G>A
ENST00000256592.2:c.-1-59G>A ENSP00000256592.1:n.-1-59G>A
NM_000549.4:c.-1-59G>A NP_000540.2:n.-1-59G>A
XM_011542065.1:c.-60G>A XP_011540367.1:n.-60G>A
XM_011542065.2:c.-60G>A XP_011540367.1:n.-60G>A
NM_000549.5:c.-1-59G>A MANE Select NP_000540.2:n.-1-59G>A
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