Canonical Allele Identifier: CA4885899

Gene: TG

Linked Data

• dbSNP Id: rs745673880
• ExAC: 8:134145838 C / T
• gnomAD v2: 8-134145838-C-T
• gnomAD v4: 8-133133594-C-T
• MyVariant Identifiers: chr8:g.134145838C>T (hg19) ; chr8:g.133133594C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133594C>T , CM000670.2:g.133133594C>T	GRCh38
NC_000008.10:g.134145838C>T , CM000670.1:g.134145838C>T	GRCh37
NC_000008.9:g.134215020C>T	NCBI36
NG_015832.1:g.271634C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8122C>T MANE Select	ENSP00000220616.4:p.Gln2708Ter
ENST00000220616.8:c.8122C>T	ENSP00000220616.4:p.Gln2708Ter
ENST00000519178.5:c.3488C>T
ENST00000519543.5:c.2521C>T	ENSP00000430430.1:p.Gln841Ter
ENST00000521107.1:c.334C>T	ENSP00000430161.1:p.Gln112Ter
ENST00000522691.1:n.208C>T
ENST00000523756.5:c.4777C>T
NM_003235.4:c.8122C>T	NP_003226.4:p.Gln2708Ter
XM_005251038.3:c.7930C>T	XP_005251095.1:p.Gln2644Ter
XM_006716622.2:c.8059C>T	XP_006716685.1:p.Gln2687Ter
XM_005251038.4:c.7930C>T	XP_005251095.1:p.Gln2644Ter
XM_006716622.3:c.8059C>T	XP_006716685.1:p.Gln2687Ter
XM_017013793.1:c.8056C>T	XP_016869282.1:p.Gln2686Ter
XM_017013794.1:c.7987C>T	XP_016869283.1:p.Gln2663Ter
XM_017013795.1:c.7951C>T	XP_016869284.1:p.Gln2651Ter
XM_017013796.1:c.7903C>T	XP_016869285.1:p.Gln2635Ter
XM_017013797.1:c.7861C>T	XP_016869286.1:p.Gln2621Ter
NM_003235.5:c.8122C>T MANE Select	NP_003226.4:p.Gln2708Ter