Canonical Allele Identifier: CA186356498

Gene: TG

Linked Data

• dbSNP Id: rs151314518
• gnomAD v2: 8-134145523-G-T
• gnomAD v3: 8-133133279-G-T
• gnomAD v4: 8-133133279-G-T
• MyVariant Identifiers: chr8:g.134145523G>T (hg19) ; chr8:g.133133279G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133279G>T , CM000670.2:g.133133279G>T	GRCh38
NC_000008.10:g.134145523G>T , CM000670.1:g.134145523G>T	GRCh37
NC_000008.9:g.134214705G>T	NCBI36
NG_015832.1:g.271319G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.7998-191G>T MANE Select	ENSP00000220616.4:n.7998-191G>T
ENST00000220616.8:c.7998-191G>T	ENSP00000220616.4:n.7998-191G>T
ENST00000519178.5:c.3364-191G>T
ENST00000519543.5:c.2397-191G>T	ENSP00000430430.1:n.2397-191G>T
ENST00000521107.1:c.210-191G>T	ENSP00000430161.1:n.210-191G>T
ENST00000523756.5:c.4653-191G>T
NM_003235.4:c.7998-191G>T	NP_003226.4:n.7998-191G>T
XM_005251038.3:c.7806-191G>T	XP_005251095.1:n.7806-191G>T
XM_006716622.2:c.7935-191G>T	XP_006716685.1:n.7935-191G>T
XM_005251038.4:c.7806-191G>T	XP_005251095.1:n.7806-191G>T
XM_006716622.3:c.7935-191G>T	XP_006716685.1:n.7935-191G>T
XM_017013793.1:c.7932-191G>T	XP_016869282.1:n.7932-191G>T
XM_017013794.1:c.7863-191G>T	XP_016869283.1:n.7863-191G>T
XM_017013795.1:c.7827-191G>T	XP_016869284.1:n.7827-191G>T
XM_017013796.1:c.7779-191G>T	XP_016869285.1:n.7779-191G>T
XM_017013797.1:c.7737-191G>T	XP_016869286.1:n.7737-191G>T
NM_003235.5:c.7998-191G>T MANE Select	NP_003226.4:n.7998-191G>T