Canonical Allele Identifier: CA2647270460
Gene: TSHB HGNC NCBI

Linked Data

gnomAD v4: 1-115033828-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033828T>G , CM000663.2:g.115033828T>G GRCh38
NC_000001.10:g.115576449T>G , CM000663.1:g.115576449T>G GRCh37
NC_000001.9:g.115377972T>G NCBI36
NG_015891.1:g.9035T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.163-145T>G MANE Select ENSP00000256592.1:n.163-145T>G
ENST00000256592.2:c.163-145T>G ENSP00000256592.1:n.163-145T>G
ENST00000369517.1:c.163-145T>G ENSP00000358530.1:n.163-145T>G
NM_000549.4:c.163-145T>G NP_000540.2:n.163-145T>G
XM_011542065.1:c.163-145T>G XP_011540367.1:n.163-145T>G
XM_011542065.2:c.163-145T>G XP_011540367.1:n.163-145T>G
NM_000549.5:c.163-145T>G MANE Select NP_000540.2:n.163-145T>G
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