Canonical Allele Identifier: CA1022541
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs780156171

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033552C>G , CM000663.2:g.115033552C>G GRCh38
NC_000001.10:g.115576173C>G , CM000663.1:g.115576173C>G GRCh37
NC_000001.9:g.115377696C>G NCBI36
NG_015891.1:g.8759C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.162+28C>G MANE Select ENSP00000256592.1:n.162+28C>G
ENST00000256592.2:c.162+28C>G ENSP00000256592.1:n.162+28C>G
ENST00000369517.1:c.162+28C>G ENSP00000358530.1:n.162+28C>G
NM_000549.4:c.162+28C>G NP_000540.2:n.162+28C>G
XM_011542065.1:c.162+28C>G XP_011540367.1:n.162+28C>G
XM_011542065.2:c.162+28C>G XP_011540367.1:n.162+28C>G
NM_000549.5:c.162+28C>G MANE Select NP_000540.2:n.162+28C>G