Canonical Allele Identifier: CA4885893

Gene: TG

Linked Data

• dbSNP Id: rs561370673
• ExAC: 8:134145809 A / G
• gnomAD v2: 8-134145809-A-G
• gnomAD v3: 8-133133565-A-G
• gnomAD v4: 8-133133565-A-G
• MyVariant Identifiers: chr8:g.134145809A>G (hg19) ; chr8:g.133133565A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133565A>G , CM000670.2:g.133133565A>G	GRCh38
NC_000008.10:g.134145809A>G , CM000670.1:g.134145809A>G	GRCh37
NC_000008.9:g.134214991A>G	NCBI36
NG_015832.1:g.271605A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8093A>G MANE Select	ENSP00000220616.4:p.Lys2698Arg
ENST00000220616.8:c.8093A>G	ENSP00000220616.4:p.Lys2698Arg
ENST00000519178.5:c.3459A>G
ENST00000519543.5:c.2492A>G	ENSP00000430430.1:p.Lys831Arg
ENST00000521107.1:c.305A>G	ENSP00000430161.1:p.Lys102Arg
ENST00000522691.1:n.179A>G
ENST00000523756.5:c.4748A>G
NM_003235.4:c.8093A>G	NP_003226.4:p.Lys2698Arg
XM_005251038.3:c.7901A>G	XP_005251095.1:p.Lys2634Arg
XM_006716622.2:c.8030A>G	XP_006716685.1:p.Lys2677Arg
XM_005251038.4:c.7901A>G	XP_005251095.1:p.Lys2634Arg
XM_006716622.3:c.8030A>G	XP_006716685.1:p.Lys2677Arg
XM_017013793.1:c.8027A>G	XP_016869282.1:p.Lys2676Arg
XM_017013794.1:c.7958A>G	XP_016869283.1:p.Lys2653Arg
XM_017013795.1:c.7922A>G	XP_016869284.1:p.Lys2641Arg
XM_017013796.1:c.7874A>G	XP_016869285.1:p.Lys2625Arg
XM_017013797.1:c.7832A>G	XP_016869286.1:p.Lys2611Arg
NM_003235.5:c.8093A>G MANE Select	NP_003226.4:p.Lys2698Arg