Canonical Allele Identifier: CA419891290
Gene: TSHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115576019C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033398C>A , CM000663.2:g.115033398C>A GRCh38
NC_000001.10:g.115576019C>A , CM000663.1:g.115576019C>A GRCh37
NC_000001.9:g.115377542C>A NCBI36
NG_015891.1:g.8605C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256592.3:c.36C>A MANE Select ENSP00000256592.1:p.Gly12=
ENST00000256592.2:c.36C>A ENSP00000256592.1:p.Gly12=
ENST00000369517.1:c.36C>A ENSP00000358530.1:p.Gly12=
NM_000549.4:c.36C>A NP_000540.2:p.Gly12=
XM_011542065.1:c.36C>A XP_011540367.1:p.Gly12=
XM_011542065.2:c.36C>A XP_011540367.1:p.Gly12=
NM_000549.5:c.36C>A MANE Select NP_000540.2:p.Gly12=