Canonical Allele Identifier: CA372253605

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145872C>G (hg19) ; chr8:g.133133628C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133628C>G , CM000670.2:g.133133628C>G	GRCh38
NC_000008.10:g.134145872C>G , CM000670.1:g.134145872C>G	GRCh37
NC_000008.9:g.134215054C>G	NCBI36
NG_015832.1:g.271668C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8156C>G MANE Select	ENSP00000220616.4:p.Ser2719Cys
ENST00000220616.8:c.8156C>G	ENSP00000220616.4:p.Ser2719Cys
ENST00000519178.5:c.3522C>G
ENST00000519543.5:c.2555C>G	ENSP00000430430.1:p.Ser852Cys
ENST00000521107.1:c.368C>G	ENSP00000430161.1:p.Ser123Cys
ENST00000522691.1:n.242C>G
ENST00000523756.5:c.4811C>G
NM_003235.4:c.8156C>G	NP_003226.4:p.Ser2719Cys
XM_005251038.3:c.7964C>G	XP_005251095.1:p.Ser2655Cys
XM_006716622.2:c.8093C>G	XP_006716685.1:p.Ser2698Cys
XM_005251038.4:c.7964C>G	XP_005251095.1:p.Ser2655Cys
XM_006716622.3:c.8093C>G	XP_006716685.1:p.Ser2698Cys
XM_017013793.1:c.8090C>G	XP_016869282.1:p.Ser2697Cys
XM_017013794.1:c.8021C>G	XP_016869283.1:p.Ser2674Cys
XM_017013795.1:c.7985C>G	XP_016869284.1:p.Ser2662Cys
XM_017013796.1:c.7937C>G	XP_016869285.1:p.Ser2646Cys
XM_017013797.1:c.7895C>G	XP_016869286.1:p.Ser2632Cys
NM_003235.5:c.8156C>G MANE Select	NP_003226.4:p.Ser2719Cys