Canonical Allele Identifier: CA419891297
Gene: TSHB HGNC NCBI

Linked Data

dbSNP Id: rs2101008607
MyVariant Identifiers: chr1:g.115576031G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.115033410G>T , CM000663.2:g.115033410G>T GRCh38
NC_000001.10:g.115576031G>T , CM000663.1:g.115576031G>T GRCh37
NC_000001.9:g.115377554G>T NCBI36
NG_015891.1:g.8617G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256592.3:c.48G>T MANE Select ENSP00000256592.1:p.Gly16=
ENST00000256592.2:c.48G>T ENSP00000256592.1:p.Gly16=
ENST00000369517.1:c.48G>T ENSP00000358530.1:p.Gly16=
NM_000549.4:c.48G>T NP_000540.2:p.Gly16=
XM_011542065.1:c.48G>T XP_011540367.1:p.Gly16=
XM_011542065.2:c.48G>T XP_011540367.1:p.Gly16=
NM_000549.5:c.48G>T MANE Select NP_000540.2:p.Gly16=