Canonical Allele Identifier: CA585277913

Gene: TG

Linked Data

• dbSNP Id: rs1300002238
• gnomAD v2: 8-134145913-G-T
• MyVariant Identifiers: chr8:g.134145913G>T (hg19) ; chr8:g.133133669G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133669G>T , CM000670.2:g.133133669G>T	GRCh38
NC_000008.10:g.134145913G>T , CM000670.1:g.134145913G>T	GRCh37
NC_000008.9:g.134215095G>T	NCBI36
NG_015832.1:g.271709G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8188+9G>T MANE Select	ENSP00000220616.4:n.8188+9G>T
ENST00000220616.8:c.8188+9G>T	ENSP00000220616.4:n.8188+9G>T
ENST00000519178.5:c.3554+9G>T
ENST00000519543.5:c.2587+9G>T	ENSP00000430430.1:n.2587+9G>T
ENST00000521107.1:c.400+9G>T	ENSP00000430161.1:n.400+9G>T
ENST00000522691.1:n.274+9G>T
ENST00000523756.5:c.4843+9G>T
NM_003235.4:c.8188+9G>T	NP_003226.4:n.8188+9G>T
XM_005251038.3:c.7996+9G>T	XP_005251095.1:n.7996+9G>T
XM_006716622.2:c.8125+9G>T	XP_006716685.1:n.8125+9G>T
XM_005251038.4:c.7996+9G>T	XP_005251095.1:n.7996+9G>T
XM_006716622.3:c.8125+9G>T	XP_006716685.1:n.8125+9G>T
XM_017013793.1:c.8122+9G>T	XP_016869282.1:n.8122+9G>T
XM_017013794.1:c.8053+9G>T	XP_016869283.1:n.8053+9G>T
XM_017013795.1:c.8017+9G>T	XP_016869284.1:n.8017+9G>T
XM_017013796.1:c.7969+9G>T	XP_016869285.1:n.7969+9G>T
XM_017013797.1:c.7927+9G>T	XP_016869286.1:n.7927+9G>T
NM_003235.5:c.8188+9G>T MANE Select	NP_003226.4:n.8188+9G>T