Canonical Allele Identifier: CA341755036
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs926850907

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033457A>C , CM000663.2:g.115033457A>C GRCh38
NC_000001.10:g.115576078A>C , CM000663.1:g.115576078A>C GRCh37
NC_000001.9:g.115377601A>C NCBI36
NG_015891.1:g.8664A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.95A>C MANE Select ENSP00000256592.1:p.Glu32Ala
ENST00000256592.2:c.95A>C ENSP00000256592.1:p.Glu32Ala
ENST00000369517.1:c.95A>C ENSP00000358530.1:p.Glu32Ala
NM_000549.4:c.95A>C NP_000540.2:p.Glu32Ala
XM_011542065.1:c.95A>C XP_011540367.1:p.Glu32Ala
XM_011542065.2:c.95A>C XP_011540367.1:p.Glu32Ala
NM_000549.5:c.95A>C MANE Select NP_000540.2:p.Glu32Ala