Canonical Allele Identifier: CA372253631
Gene: TG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133133634A>C , CM000670.2:g.133133634A>C GRCh38
NC_000008.10:g.134145878A>C , CM000670.1:g.134145878A>C GRCh37
NC_000008.9:g.134215060A>C NCBI36
NG_015832.1:g.271674A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.8162A>C MANE Select ENSP00000220616.4:p.Tyr2721Ser
ENST00000220616.8:c.8162A>C ENSP00000220616.4:p.Tyr2721Ser
ENST00000519178.5:c.3528A>C
ENST00000519543.5:c.2561A>C ENSP00000430430.1:p.Tyr854Ser
ENST00000521107.1:c.374A>C ENSP00000430161.1:p.Tyr125Ser
ENST00000522691.1:n.248A>C
ENST00000523756.5:c.4817A>C
NM_003235.4:c.8162A>C NP_003226.4:p.Tyr2721Ser
XM_005251038.3:c.7970A>C XP_005251095.1:p.Tyr2657Ser
XM_006716622.2:c.8099A>C XP_006716685.1:p.Tyr2700Ser
XM_005251038.4:c.7970A>C XP_005251095.1:p.Tyr2657Ser
XM_006716622.3:c.8099A>C XP_006716685.1:p.Tyr2700Ser
XM_017013793.1:c.8096A>C XP_016869282.1:p.Tyr2699Ser
XM_017013794.1:c.8027A>C XP_016869283.1:p.Tyr2676Ser
XM_017013795.1:c.7991A>C XP_016869284.1:p.Tyr2664Ser
XM_017013796.1:c.7943A>C XP_016869285.1:p.Tyr2648Ser
XM_017013797.1:c.7901A>C XP_016869286.1:p.Tyr2634Ser
NM_003235.5:c.8162A>C MANE Select NP_003226.4:p.Tyr2721Ser