Canonical Allele Identifier: CA463016988

Gene: TG

Linked Data

• gnomAD v4: 8-133133479-C-T
• MyVariant Identifiers: chr8:g.134145723C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133479C>T , CM000670.2:g.133133479C>T	GRCh38
NC_000008.10:g.134145723C>T , CM000670.1:g.134145723C>T	GRCh37
NC_000008.9:g.134214905C>T	NCBI36
NG_015832.1:g.271519C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8007C>T MANE Select	ENSP00000220616.4:p.Asn2669=
ENST00000220616.8:c.8007C>T	ENSP00000220616.4:p.Asn2669=
ENST00000519178.5:c.3373C>T
ENST00000519543.5:c.2406C>T	ENSP00000430430.1:p.Asn802=
ENST00000521107.1:c.219C>T	ENSP00000430161.1:p.Asn73=
ENST00000522691.1:n.93C>T
ENST00000523756.5:c.4662C>T
NM_003235.4:c.8007C>T	NP_003226.4:p.Asn2669=
XM_005251038.3:c.7815C>T	XP_005251095.1:p.Asn2605=
XM_006716622.2:c.7944C>T	XP_006716685.1:p.Asn2648=
XM_005251038.4:c.7815C>T	XP_005251095.1:p.Asn2605=
XM_006716622.3:c.7944C>T	XP_006716685.1:p.Asn2648=
XM_017013793.1:c.7941C>T	XP_016869282.1:p.Asn2647=
XM_017013794.1:c.7872C>T	XP_016869283.1:p.Asn2624=
XM_017013795.1:c.7836C>T	XP_016869284.1:p.Asn2612=
XM_017013796.1:c.7788C>T	XP_016869285.1:p.Asn2596=
XM_017013797.1:c.7746C>T	XP_016869286.1:p.Asn2582=
NM_003235.5:c.8007C>T MANE Select	NP_003226.4:p.Asn2669=