Canonical Allele Identifier: CA341754633
Gene: TSHB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033394T>C , CM000663.2:g.115033394T>C GRCh38
NC_000001.10:g.115576015T>C , CM000663.1:g.115576015T>C GRCh37
NC_000001.9:g.115377538T>C NCBI36
NG_015891.1:g.8601T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.32T>C MANE Select ENSP00000256592.1:p.Phe11Ser
ENST00000256592.2:c.32T>C ENSP00000256592.1:p.Phe11Ser
ENST00000369517.1:c.32T>C ENSP00000358530.1:p.Phe11Ser
NM_000549.4:c.32T>C NP_000540.2:p.Phe11Ser
XM_011542065.1:c.32T>C XP_011540367.1:p.Phe11Ser
XM_011542065.2:c.32T>C XP_011540367.1:p.Phe11Ser
NM_000549.5:c.32T>C MANE Select NP_000540.2:p.Phe11Ser