Canonical Allele Identifier: CA847740790

Gene: TG

Linked Data

• dbSNP Id: rs1293138766
• MyVariant Identifiers: chr8:g.134145532G>C (hg19) ; chr8:g.133133288G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133288G>C , CM000670.2:g.133133288G>C	GRCh38
NC_000008.10:g.134145532G>C , CM000670.1:g.134145532G>C	GRCh37
NC_000008.9:g.134214714G>C	NCBI36
NG_015832.1:g.271328G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.7998-182G>C MANE Select	ENSP00000220616.4:n.7998-182G>C
ENST00000220616.8:c.7998-182G>C	ENSP00000220616.4:n.7998-182G>C
ENST00000519178.5:c.3364-182G>C
ENST00000519543.5:c.2397-182G>C	ENSP00000430430.1:n.2397-182G>C
ENST00000521107.1:c.210-182G>C	ENSP00000430161.1:n.210-182G>C
ENST00000523756.5:c.4653-182G>C
NM_003235.4:c.7998-182G>C	NP_003226.4:n.7998-182G>C
XM_005251038.3:c.7806-182G>C	XP_005251095.1:n.7806-182G>C
XM_006716622.2:c.7935-182G>C	XP_006716685.1:n.7935-182G>C
XM_005251038.4:c.7806-182G>C	XP_005251095.1:n.7806-182G>C
XM_006716622.3:c.7935-182G>C	XP_006716685.1:n.7935-182G>C
XM_017013793.1:c.7932-182G>C	XP_016869282.1:n.7932-182G>C
XM_017013794.1:c.7863-182G>C	XP_016869283.1:n.7863-182G>C
XM_017013795.1:c.7827-182G>C	XP_016869284.1:n.7827-182G>C
XM_017013796.1:c.7779-182G>C	XP_016869285.1:n.7779-182G>C
XM_017013797.1:c.7737-182G>C	XP_016869286.1:n.7737-182G>C
NM_003235.5:c.7998-182G>C MANE Select	NP_003226.4:n.7998-182G>C