Canonical Allele Identifier: CA341754712
Gene: TSHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033413A>C , CM000663.2:g.115033413A>C GRCh38
NC_000001.10:g.115576034A>C , CM000663.1:g.115576034A>C GRCh37
NC_000001.9:g.115377557A>C NCBI36
NG_015891.1:g.8620A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.51A>C MANE Select ENSP00000256592.1:p.Gln17His
ENST00000256592.2:c.51A>C ENSP00000256592.1:p.Gln17His
ENST00000369517.1:c.51A>C ENSP00000358530.1:p.Gln17His
NM_000549.4:c.51A>C NP_000540.2:p.Gln17His
XM_011542065.1:c.51A>C XP_011540367.1:p.Gln17His
XM_011542065.2:c.51A>C XP_011540367.1:p.Gln17His
NM_000549.5:c.51A>C MANE Select NP_000540.2:p.Gln17His