Canonical Allele Identifier: CA4885904

Gene: TG

Linked Data

• dbSNP Id: rs774585616
• ExAC: 8:134145860 G / C
• gnomAD v2: 8-134145860-G-C
• gnomAD v4: 8-133133616-G-C
• MyVariant Identifiers: chr8:g.134145860G>C (hg19) ; chr8:g.133133616G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133616G>C , CM000670.2:g.133133616G>C	GRCh38
NC_000008.10:g.134145860G>C , CM000670.1:g.134145860G>C	GRCh37
NC_000008.9:g.134215042G>C	NCBI36
NG_015832.1:g.271656G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8144G>C MANE Select	ENSP00000220616.4:p.Cys2715Ser
ENST00000220616.8:c.8144G>C	ENSP00000220616.4:p.Cys2715Ser
ENST00000519178.5:c.3510G>C
ENST00000519543.5:c.2543G>C	ENSP00000430430.1:p.Cys848Ser
ENST00000521107.1:c.356G>C	ENSP00000430161.1:p.Cys119Ser
ENST00000522691.1:n.230G>C
ENST00000523756.5:c.4799G>C
NM_003235.4:c.8144G>C	NP_003226.4:p.Cys2715Ser
XM_005251038.3:c.7952G>C	XP_005251095.1:p.Cys2651Ser
XM_006716622.2:c.8081G>C	XP_006716685.1:p.Cys2694Ser
XM_005251038.4:c.7952G>C	XP_005251095.1:p.Cys2651Ser
XM_006716622.3:c.8081G>C	XP_006716685.1:p.Cys2694Ser
XM_017013793.1:c.8078G>C	XP_016869282.1:p.Cys2693Ser
XM_017013794.1:c.8009G>C	XP_016869283.1:p.Cys2670Ser
XM_017013795.1:c.7973G>C	XP_016869284.1:p.Cys2658Ser
XM_017013796.1:c.7925G>C	XP_016869285.1:p.Cys2642Ser
XM_017013797.1:c.7883G>C	XP_016869286.1:p.Cys2628Ser
NM_003235.5:c.8144G>C MANE Select	NP_003226.4:p.Cys2715Ser