Canonical Allele Identifier: CA2688665086

Gene: TG

Linked Data

• gnomAD v4: 8-133133241-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133241C>G , CM000670.2:g.133133241C>G	GRCh38
NC_000008.10:g.134145485C>G , CM000670.1:g.134145485C>G	GRCh37
NC_000008.9:g.134214667C>G	NCBI36
NG_015832.1:g.271281C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.7998-229C>G MANE Select	ENSP00000220616.4:n.7998-229C>G
ENST00000220616.8:c.7998-229C>G	ENSP00000220616.4:n.7998-229C>G
ENST00000519178.5:c.3364-229C>G
ENST00000519543.5:c.2397-229C>G	ENSP00000430430.1:n.2397-229C>G
ENST00000521107.1:c.210-229C>G	ENSP00000430161.1:n.210-229C>G
ENST00000523756.5:c.4653-229C>G
NM_003235.4:c.7998-229C>G	NP_003226.4:n.7998-229C>G
XM_005251038.3:c.7806-229C>G	XP_005251095.1:n.7806-229C>G
XM_006716622.2:c.7935-229C>G	XP_006716685.1:n.7935-229C>G
XM_005251038.4:c.7806-229C>G	XP_005251095.1:n.7806-229C>G
XM_006716622.3:c.7935-229C>G	XP_006716685.1:n.7935-229C>G
XM_017013793.1:c.7932-229C>G	XP_016869282.1:n.7932-229C>G
XM_017013794.1:c.7863-229C>G	XP_016869283.1:n.7863-229C>G
XM_017013795.1:c.7827-229C>G	XP_016869284.1:n.7827-229C>G
XM_017013796.1:c.7779-229C>G	XP_016869285.1:n.7779-229C>G
XM_017013797.1:c.7737-229C>G	XP_016869286.1:n.7737-229C>G
NM_003235.5:c.7998-229C>G MANE Select	NP_003226.4:n.7998-229C>G