Canonical Allele Identifier: CA186356470

Gene: TG

Linked Data

• dbSNP Id: rs1044652807
• gnomAD v2: 8-134145453-G-A
• gnomAD v3: 8-133133209-G-A
• gnomAD v4: 8-133133209-G-A
• MyVariant Identifiers: chr8:g.134145453G>A (hg19) ; chr8:g.133133209G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133209G>A , CM000670.2:g.133133209G>A	GRCh38
NC_000008.10:g.134145453G>A , CM000670.1:g.134145453G>A	GRCh37
NC_000008.9:g.134214635G>A	NCBI36
NG_015832.1:g.271249G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.7998-261G>A MANE Select	ENSP00000220616.4:n.7998-261G>A
ENST00000220616.8:c.7998-261G>A	ENSP00000220616.4:n.7998-261G>A
ENST00000519178.5:c.3364-261G>A
ENST00000519543.5:c.2397-261G>A	ENSP00000430430.1:n.2397-261G>A
ENST00000521107.1:c.210-261G>A	ENSP00000430161.1:n.210-261G>A
ENST00000523756.5:c.4653-261G>A
NM_003235.4:c.7998-261G>A	NP_003226.4:n.7998-261G>A
XM_005251038.3:c.7806-261G>A	XP_005251095.1:n.7806-261G>A
XM_006716622.2:c.7935-261G>A	XP_006716685.1:n.7935-261G>A
XM_005251038.4:c.7806-261G>A	XP_005251095.1:n.7806-261G>A
XM_006716622.3:c.7935-261G>A	XP_006716685.1:n.7935-261G>A
XM_017013793.1:c.7932-261G>A	XP_016869282.1:n.7932-261G>A
XM_017013794.1:c.7863-261G>A	XP_016869283.1:n.7863-261G>A
XM_017013795.1:c.7827-261G>A	XP_016869284.1:n.7827-261G>A
XM_017013796.1:c.7779-261G>A	XP_016869285.1:n.7779-261G>A
XM_017013797.1:c.7737-261G>A	XP_016869286.1:n.7737-261G>A
NM_003235.5:c.7998-261G>A MANE Select	NP_003226.4:n.7998-261G>A