Canonical Allele Identifier: CA372247122

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.133885313G>C (hg19) ; chr8:g.132873068G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132873068G>C , CM000670.2:g.132873068G>C	GRCh38
NC_000008.10:g.133885313G>C , CM000670.1:g.133885313G>C	GRCh37
NC_000008.9:g.133954495G>C	NCBI36
NG_015832.1:g.11109G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.485G>C MANE Select	ENSP00000220616.4:p.Arg162Thr
ENST00000220616.8:c.485G>C	ENSP00000220616.4:p.Arg162Thr
ENST00000523901.1:c.*336G>C	ENSP00000427871.1:n.*336G>C
NM_003235.4:c.485G>C	NP_003226.4:p.Arg162Thr
XM_005251038.3:c.485G>C	XP_005251095.1:p.Arg162Thr
XM_005251040.3:c.485G>C	XP_005251097.1:p.Arg162Thr
XM_005251042.3:c.485G>C	XP_005251099.1:p.Arg162Thr
XM_005251043.3:c.485G>C	XP_005251100.1:p.Arg162Thr
XM_006716622.2:c.485G>C	XP_006716685.1:p.Arg162Thr
XM_005251038.4:c.485G>C	XP_005251095.1:p.Arg162Thr
XM_005251040.4:c.485G>C	XP_005251097.1:p.Arg162Thr
XM_005251042.4:c.485G>C	XP_005251099.1:p.Arg162Thr
XM_006716622.3:c.485G>C	XP_006716685.1:p.Arg162Thr
XM_017013793.1:c.485G>C	XP_016869282.1:p.Arg162Thr
XM_017013794.1:c.485G>C	XP_016869283.1:p.Arg162Thr
XM_017013795.1:c.485G>C	XP_016869284.1:p.Arg162Thr
XM_017013796.1:c.485G>C	XP_016869285.1:p.Arg162Thr
XM_017013797.1:c.224G>C	XP_016869286.1:p.Arg75Thr
XM_017013798.1:c.485G>C	XP_016869287.1:p.Arg162Thr
XM_017013799.1:c.485G>C	XP_016869288.1:p.Arg162Thr
XM_017013800.1:c.485G>C	XP_016869289.1:p.Arg162Thr
NM_003235.5:c.485G>C MANE Select	NP_003226.4:p.Arg162Thr