Canonical Allele Identifier: CA186356863

Gene: TG

Linked Data

• dbSNP Id: rs1055215249
• gnomAD v2: 8-134145856-G-A
• gnomAD v3: 8-133133612-G-A
• gnomAD v4: 8-133133612-G-A
• MyVariant Identifiers: chr8:g.134145856G>A (hg19) ; chr8:g.133133612G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133612G>A , CM000670.2:g.133133612G>A	GRCh38
NC_000008.10:g.134145856G>A , CM000670.1:g.134145856G>A	GRCh37
NC_000008.9:g.134215038G>A	NCBI36
NG_015832.1:g.271652G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8140G>A MANE Select	ENSP00000220616.4:p.Asp2714Asn
ENST00000220616.8:c.8140G>A	ENSP00000220616.4:p.Asp2714Asn
ENST00000519178.5:c.3506G>A
ENST00000519543.5:c.2539G>A	ENSP00000430430.1:p.Asp847Asn
ENST00000521107.1:c.352G>A	ENSP00000430161.1:p.Asp118Asn
ENST00000522691.1:n.226G>A
ENST00000523756.5:c.4795G>A
NM_003235.4:c.8140G>A	NP_003226.4:p.Asp2714Asn
XM_005251038.3:c.7948G>A	XP_005251095.1:p.Asp2650Asn
XM_006716622.2:c.8077G>A	XP_006716685.1:p.Asp2693Asn
XM_005251038.4:c.7948G>A	XP_005251095.1:p.Asp2650Asn
XM_006716622.3:c.8077G>A	XP_006716685.1:p.Asp2693Asn
XM_017013793.1:c.8074G>A	XP_016869282.1:p.Asp2692Asn
XM_017013794.1:c.8005G>A	XP_016869283.1:p.Asp2669Asn
XM_017013795.1:c.7969G>A	XP_016869284.1:p.Asp2657Asn
XM_017013796.1:c.7921G>A	XP_016869285.1:p.Asp2641Asn
XM_017013797.1:c.7879G>A	XP_016869286.1:p.Asp2627Asn
NM_003235.5:c.8140G>A MANE Select	NP_003226.4:p.Asp2714Asn