Canonical Allele Identifier: CA4885023

Gene: TG

Linked Data

• dbSNP Id: rs761874763
• ExAC: 8:134030280 G / C
• gnomAD v2: 8-134030280-G-C
• gnomAD v4: 8-133018035-G-C
• MyVariant Identifiers: chr8:g.134030280G>C (hg19) ; chr8:g.133018035G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133018035G>C , CM000670.2:g.133018035G>C	GRCh38
NC_000008.10:g.134030280G>C , CM000670.1:g.134030280G>C	GRCh37
NC_000008.9:g.134099462G>C	NCBI36
NG_015832.1:g.156076G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6782+38G>C MANE Select	ENSP00000220616.4:n.6782+38G>C
ENST00000220616.8:c.6782+38G>C	ENSP00000220616.4:n.6782+38G>C
ENST00000518108.1:c.168+169G>C
ENST00000519178.5:c.2148+38G>C
ENST00000519543.5:c.1181+38G>C	ENSP00000430430.1:n.1181+38G>C
ENST00000523756.5:c.3437+38G>C
NM_003235.4:c.6782+38G>C	NP_003226.4:n.6782+38G>C
XM_005251038.3:c.6590+38G>C	XP_005251095.1:n.6590+38G>C
XM_006716622.2:c.6719+38G>C	XP_006716685.1:n.6719+38G>C
XM_005251038.4:c.6590+38G>C	XP_005251095.1:n.6590+38G>C
XM_006716622.3:c.6719+38G>C	XP_006716685.1:n.6719+38G>C
XM_017013793.1:c.6716+38G>C	XP_016869282.1:n.6716+38G>C
XM_017013794.1:c.6782+38G>C	XP_016869283.1:n.6782+38G>C
XM_017013795.1:c.6611+38G>C	XP_016869284.1:n.6611+38G>C
XM_017013796.1:c.6563+38G>C	XP_016869285.1:n.6563+38G>C
XM_017013797.1:c.6521+38G>C	XP_016869286.1:n.6521+38G>C
XM_017013798.1:c.6782+38G>C	XP_016869287.1:n.6782+38G>C
NM_003235.5:c.6782+38G>C MANE Select	NP_003226.4:n.6782+38G>C