Canonical Allele Identifier: CA186356957

Gene: TG

Linked Data

• dbSNP Id: rs1046477999
• MyVariant Identifiers: chr8:g.134145894G>T (hg19) ; chr8:g.133133650G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133650G>T , CM000670.2:g.133133650G>T	GRCh38
NC_000008.10:g.134145894G>T , CM000670.1:g.134145894G>T	GRCh37
NC_000008.9:g.134215076G>T	NCBI36
NG_015832.1:g.271690G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8178G>T MANE Select	ENSP00000220616.4:p.Lys2726Asn
ENST00000220616.8:c.8178G>T	ENSP00000220616.4:p.Lys2726Asn
ENST00000519178.5:c.3544G>T
ENST00000519543.5:c.2577G>T	ENSP00000430430.1:p.Lys859Asn
ENST00000521107.1:c.390G>T	ENSP00000430161.1:p.Lys130Asn
ENST00000522691.1:n.264G>T
ENST00000523756.5:c.4833G>T
NM_003235.4:c.8178G>T	NP_003226.4:p.Lys2726Asn
XM_005251038.3:c.7986G>T	XP_005251095.1:p.Lys2662Asn
XM_006716622.2:c.8115G>T	XP_006716685.1:p.Lys2705Asn
XM_005251038.4:c.7986G>T	XP_005251095.1:p.Lys2662Asn
XM_006716622.3:c.8115G>T	XP_006716685.1:p.Lys2705Asn
XM_017013793.1:c.8112G>T	XP_016869282.1:p.Lys2704Asn
XM_017013794.1:c.8043G>T	XP_016869283.1:p.Lys2681Asn
XM_017013795.1:c.8007G>T	XP_016869284.1:p.Lys2669Asn
XM_017013796.1:c.7959G>T	XP_016869285.1:p.Lys2653Asn
XM_017013797.1:c.7917G>T	XP_016869286.1:p.Lys2639Asn
NM_003235.5:c.8178G>T MANE Select	NP_003226.4:p.Lys2726Asn