Canonical Allele Identifier: CA4885906

Gene: TG

Linked Data

• dbSNP Id: rs772485045
• ExAC: 8:134145872 C / A
• gnomAD v2: 8-134145872-C-A
• gnomAD v4: 8-133133628-C-A
• MyVariant Identifiers: chr8:g.134145872C>A (hg19) ; chr8:g.133133628C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8156C>A MANE Select	ENSP00000220616.4:p.Ser2719Tyr
ENST00000220616.8:c.8156C>A	ENSP00000220616.4:p.Ser2719Tyr
ENST00000519178.5:c.3522C>A
ENST00000519543.5:c.2555C>A	ENSP00000430430.1:p.Ser852Tyr
ENST00000521107.1:c.368C>A	ENSP00000430161.1:p.Ser123Tyr
ENST00000522691.1:n.242C>A
ENST00000523756.5:c.4811C>A
NM_003235.4:c.8156C>A	NP_003226.4:p.Ser2719Tyr
XM_005251038.3:c.7964C>A	XP_005251095.1:p.Ser2655Tyr
XM_006716622.2:c.8093C>A	XP_006716685.1:p.Ser2698Tyr
XM_005251038.4:c.7964C>A	XP_005251095.1:p.Ser2655Tyr
XM_006716622.3:c.8093C>A	XP_006716685.1:p.Ser2698Tyr
XM_017013793.1:c.8090C>A	XP_016869282.1:p.Ser2697Tyr
XM_017013794.1:c.8021C>A	XP_016869283.1:p.Ser2674Tyr
XM_017013795.1:c.7985C>A	XP_016869284.1:p.Ser2662Tyr
XM_017013796.1:c.7937C>A	XP_016869285.1:p.Ser2646Tyr
XM_017013797.1:c.7895C>A	XP_016869286.1:p.Ser2632Tyr
NM_003235.5:c.8156C>A MANE Select	NP_003226.4:p.Ser2719Tyr