Canonical Allele Identifier: CA372253667

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145887C>G (hg19) ; chr8:g.133133643C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133643C>G , CM000670.2:g.133133643C>G	GRCh38
NC_000008.10:g.134145887C>G , CM000670.1:g.134145887C>G	GRCh37
NC_000008.9:g.134215069C>G	NCBI36
NG_015832.1:g.271683C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8171C>G MANE Select	ENSP00000220616.4:p.Ser2724Cys
ENST00000220616.8:c.8171C>G	ENSP00000220616.4:p.Ser2724Cys
ENST00000519178.5:c.3537C>G
ENST00000519543.5:c.2570C>G	ENSP00000430430.1:p.Ser857Cys
ENST00000521107.1:c.383C>G	ENSP00000430161.1:p.Ser128Cys
ENST00000522691.1:n.257C>G
ENST00000523756.5:c.4826C>G
NM_003235.4:c.8171C>G	NP_003226.4:p.Ser2724Cys
XM_005251038.3:c.7979C>G	XP_005251095.1:p.Ser2660Cys
XM_006716622.2:c.8108C>G	XP_006716685.1:p.Ser2703Cys
XM_005251038.4:c.7979C>G	XP_005251095.1:p.Ser2660Cys
XM_006716622.3:c.8108C>G	XP_006716685.1:p.Ser2703Cys
XM_017013793.1:c.8105C>G	XP_016869282.1:p.Ser2702Cys
XM_017013794.1:c.8036C>G	XP_016869283.1:p.Ser2679Cys
XM_017013795.1:c.8000C>G	XP_016869284.1:p.Ser2667Cys
XM_017013796.1:c.7952C>G	XP_016869285.1:p.Ser2651Cys
XM_017013797.1:c.7910C>G	XP_016869286.1:p.Ser2637Cys
NM_003235.5:c.8171C>G MANE Select	NP_003226.4:p.Ser2724Cys