Canonical Allele Identifier: CA341755059
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs1185914926

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033460G>A , CM000663.2:g.115033460G>A GRCh38
NC_000001.10:g.115576081G>A , CM000663.1:g.115576081G>A GRCh37
NC_000001.9:g.115377604G>A NCBI36
NG_015891.1:g.8667G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.98G>A MANE Select ENSP00000256592.1:p.Arg33Lys
ENST00000256592.2:c.98G>A ENSP00000256592.1:p.Arg33Lys
ENST00000369517.1:c.98G>A ENSP00000358530.1:p.Arg33Lys
NM_000549.4:c.98G>A NP_000540.2:p.Arg33Lys
XM_011542065.1:c.98G>A XP_011540367.1:p.Arg33Lys
XM_011542065.2:c.98G>A XP_011540367.1:p.Arg33Lys
NM_000549.5:c.98G>A MANE Select NP_000540.2:p.Arg33Lys