Canonical Allele Identifier: CA372247162
Gene: TG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132873085A>C , CM000670.2:g.132873085A>C GRCh38
NC_000008.10:g.133885330A>C , CM000670.1:g.133885330A>C GRCh37
NC_000008.9:g.133954512A>C NCBI36
NG_015832.1:g.11126A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.502A>C MANE Select ENSP00000220616.4:p.Asn168His
ENST00000220616.8:c.502A>C ENSP00000220616.4:p.Asn168His
ENST00000523901.1:c.*353A>C ENSP00000427871.1:n.*353A>C
NM_003235.4:c.502A>C NP_003226.4:p.Asn168His
XM_005251038.3:c.502A>C XP_005251095.1:p.Asn168His
XM_005251040.3:c.502A>C XP_005251097.1:p.Asn168His
XM_005251042.3:c.502A>C XP_005251099.1:p.Asn168His
XM_005251043.3:c.502A>C XP_005251100.1:p.Asn168His
XM_006716622.2:c.502A>C XP_006716685.1:p.Asn168His
XM_005251038.4:c.502A>C XP_005251095.1:p.Asn168His
XM_005251040.4:c.502A>C XP_005251097.1:p.Asn168His
XM_005251042.4:c.502A>C XP_005251099.1:p.Asn168His
XM_006716622.3:c.502A>C XP_006716685.1:p.Asn168His
XM_017013793.1:c.502A>C XP_016869282.1:p.Asn168His
XM_017013794.1:c.502A>C XP_016869283.1:p.Asn168His
XM_017013795.1:c.502A>C XP_016869284.1:p.Asn168His
XM_017013796.1:c.502A>C XP_016869285.1:p.Asn168His
XM_017013797.1:c.241A>C XP_016869286.1:p.Asn81His
XM_017013798.1:c.502A>C XP_016869287.1:p.Asn168His
XM_017013799.1:c.502A>C XP_016869288.1:p.Asn168His
XM_017013800.1:c.502A>C XP_016869289.1:p.Asn168His
NM_003235.5:c.502A>C MANE Select NP_003226.4:p.Asn168His