Canonical Allele Identifier: CA372252998

Gene: TG

Linked Data

• gnomAD v4: 8-133133478-A-T
• MyVariant Identifiers: chr8:g.134145722A>T (hg19) ; chr8:g.133133478A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133478A>T , CM000670.2:g.133133478A>T	GRCh38
NC_000008.10:g.134145722A>T , CM000670.1:g.134145722A>T	GRCh37
NC_000008.9:g.134214904A>T	NCBI36
NG_015832.1:g.271518A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8006A>T MANE Select	ENSP00000220616.4:p.Asn2669Ile
ENST00000220616.8:c.8006A>T	ENSP00000220616.4:p.Asn2669Ile
ENST00000519178.5:c.3372A>T
ENST00000519543.5:c.2405A>T	ENSP00000430430.1:p.Asn802Ile
ENST00000521107.1:c.218A>T	ENSP00000430161.1:p.Asn73Ile
ENST00000522691.1:n.92A>T
ENST00000523756.5:c.4661A>T
NM_003235.4:c.8006A>T	NP_003226.4:p.Asn2669Ile
XM_005251038.3:c.7814A>T	XP_005251095.1:p.Asn2605Ile
XM_006716622.2:c.7943A>T	XP_006716685.1:p.Asn2648Ile
XM_005251038.4:c.7814A>T	XP_005251095.1:p.Asn2605Ile
XM_006716622.3:c.7943A>T	XP_006716685.1:p.Asn2648Ile
XM_017013793.1:c.7940A>T	XP_016869282.1:p.Asn2647Ile
XM_017013794.1:c.7871A>T	XP_016869283.1:p.Asn2624Ile
XM_017013795.1:c.7835A>T	XP_016869284.1:p.Asn2612Ile
XM_017013796.1:c.7787A>T	XP_016869285.1:p.Asn2596Ile
XM_017013797.1:c.7745A>T	XP_016869286.1:p.Asn2582Ile
NM_003235.5:c.8006A>T MANE Select	NP_003226.4:p.Asn2669Ile