Canonical Allele Identifier: CA372253214

Gene: TG

Linked Data

• dbSNP Id: rs769942851
• gnomAD v3: 8-133133532-A-C
• gnomAD v4: 8-133133532-A-C
• MyVariant Identifiers: chr8:g.134145776A>C (hg19) ; chr8:g.133133532A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133532A>C , CM000670.2:g.133133532A>C	GRCh38
NC_000008.10:g.134145776A>C , CM000670.1:g.134145776A>C	GRCh37
NC_000008.9:g.134214958A>C	NCBI36
NG_015832.1:g.271572A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8060A>C MANE Select	ENSP00000220616.4:p.Asp2687Ala
ENST00000220616.8:c.8060A>C	ENSP00000220616.4:p.Asp2687Ala
ENST00000519178.5:c.3426A>C
ENST00000519543.5:c.2459A>C	ENSP00000430430.1:p.Asp820Ala
ENST00000521107.1:c.272A>C	ENSP00000430161.1:p.Asp91Ala
ENST00000522691.1:n.146A>C
ENST00000523756.5:c.4715A>C
NM_003235.4:c.8060A>C	NP_003226.4:p.Asp2687Ala
XM_005251038.3:c.7868A>C	XP_005251095.1:p.Asp2623Ala
XM_006716622.2:c.7997A>C	XP_006716685.1:p.Asp2666Ala
XM_005251038.4:c.7868A>C	XP_005251095.1:p.Asp2623Ala
XM_006716622.3:c.7997A>C	XP_006716685.1:p.Asp2666Ala
XM_017013793.1:c.7994A>C	XP_016869282.1:p.Asp2665Ala
XM_017013794.1:c.7925A>C	XP_016869283.1:p.Asp2642Ala
XM_017013795.1:c.7889A>C	XP_016869284.1:p.Asp2630Ala
XM_017013796.1:c.7841A>C	XP_016869285.1:p.Asp2614Ala
XM_017013797.1:c.7799A>C	XP_016869286.1:p.Asp2600Ala
NM_003235.5:c.8060A>C MANE Select	NP_003226.4:p.Asp2687Ala