Canonical Allele Identifier: CA341755374
Gene: TSHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115576131T>G (hg19) chr1:g.115033510T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033510T>G , CM000663.2:g.115033510T>G GRCh38
NC_000001.10:g.115576131T>G , CM000663.1:g.115576131T>G GRCh37
NC_000001.9:g.115377654T>G NCBI36
NG_015891.1:g.8717T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.148T>G MANE Select ENSP00000256592.1:p.Tyr50Asp
ENST00000256592.2:c.148T>G ENSP00000256592.1:p.Tyr50Asp
ENST00000369517.1:c.148T>G ENSP00000358530.1:p.Tyr50Asp
NM_000549.4:c.148T>G NP_000540.2:p.Tyr50Asp
XM_011542065.1:c.148T>G XP_011540367.1:p.Tyr50Asp
XM_011542065.2:c.148T>G XP_011540367.1:p.Tyr50Asp
NM_000549.5:c.148T>G MANE Select NP_000540.2:p.Tyr50Asp
Search 100 bp 5'
Search 100 bp 3'