Canonical Allele Identifier: CA372253466

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145840G>C (hg19) ; chr8:g.133133596G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133596G>C , CM000670.2:g.133133596G>C	GRCh38
NC_000008.10:g.134145840G>C , CM000670.1:g.134145840G>C	GRCh37
NC_000008.9:g.134215022G>C	NCBI36
NG_015832.1:g.271636G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8124G>C MANE Select	ENSP00000220616.4:p.Gln2708His
ENST00000220616.8:c.8124G>C	ENSP00000220616.4:p.Gln2708His
ENST00000519178.5:c.3490G>C
ENST00000519543.5:c.2523G>C	ENSP00000430430.1:p.Gln841His
ENST00000521107.1:c.336G>C	ENSP00000430161.1:p.Gln112His
ENST00000522691.1:n.210G>C
ENST00000523756.5:c.4779G>C
NM_003235.4:c.8124G>C	NP_003226.4:p.Gln2708His
XM_005251038.3:c.7932G>C	XP_005251095.1:p.Gln2644His
XM_006716622.2:c.8061G>C	XP_006716685.1:p.Gln2687His
XM_005251038.4:c.7932G>C	XP_005251095.1:p.Gln2644His
XM_006716622.3:c.8061G>C	XP_006716685.1:p.Gln2687His
XM_017013793.1:c.8058G>C	XP_016869282.1:p.Gln2686His
XM_017013794.1:c.7989G>C	XP_016869283.1:p.Gln2663His
XM_017013795.1:c.7953G>C	XP_016869284.1:p.Gln2651His
XM_017013796.1:c.7905G>C	XP_016869285.1:p.Gln2635His
XM_017013797.1:c.7863G>C	XP_016869286.1:p.Gln2621His
NM_003235.5:c.8124G>C MANE Select	NP_003226.4:p.Gln2708His