Canonical Allele Identifier: CA4885874

Gene: TG

Linked Data

• dbSNP Id: rs778559501
• ExAC: 8:134145724 T / A
• gnomAD v2: 8-134145724-T-A
• gnomAD v4: 8-133133480-T-A
• MyVariant Identifiers: chr8:g.134145724T>A (hg19) ; chr8:g.133133480T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133480T>A , CM000670.2:g.133133480T>A	GRCh38
NC_000008.10:g.134145724T>A , CM000670.1:g.134145724T>A	GRCh37
NC_000008.9:g.134214906T>A	NCBI36
NG_015832.1:g.271520T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8008T>A MANE Select	ENSP00000220616.4:p.Tyr2670Asn
ENST00000220616.8:c.8008T>A	ENSP00000220616.4:p.Tyr2670Asn
ENST00000519178.5:c.3374T>A
ENST00000519543.5:c.2407T>A	ENSP00000430430.1:p.Tyr803Asn
ENST00000521107.1:c.220T>A	ENSP00000430161.1:p.Tyr74Asn
ENST00000522691.1:n.94T>A
ENST00000523756.5:c.4663T>A
NM_003235.4:c.8008T>A	NP_003226.4:p.Tyr2670Asn
XM_005251038.3:c.7816T>A	XP_005251095.1:p.Tyr2606Asn
XM_006716622.2:c.7945T>A	XP_006716685.1:p.Tyr2649Asn
XM_005251038.4:c.7816T>A	XP_005251095.1:p.Tyr2606Asn
XM_006716622.3:c.7945T>A	XP_006716685.1:p.Tyr2649Asn
XM_017013793.1:c.7942T>A	XP_016869282.1:p.Tyr2648Asn
XM_017013794.1:c.7873T>A	XP_016869283.1:p.Tyr2625Asn
XM_017013795.1:c.7837T>A	XP_016869284.1:p.Tyr2613Asn
XM_017013796.1:c.7789T>A	XP_016869285.1:p.Tyr2597Asn
XM_017013797.1:c.7747T>A	XP_016869286.1:p.Tyr2583Asn
NM_003235.5:c.8008T>A MANE Select	NP_003226.4:p.Tyr2670Asn