Canonical Allele Identifier: CA372252981

Gene: TG

Linked Data

• gnomAD v4: 8-133133474-C-G
• MyVariant Identifiers: chr8:g.134145718C>G (hg19) ; chr8:g.133133474C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133474C>G , CM000670.2:g.133133474C>G	GRCh38
NC_000008.10:g.134145718C>G , CM000670.1:g.134145718C>G	GRCh37
NC_000008.9:g.134214900C>G	NCBI36
NG_015832.1:g.271514C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8002C>G MANE Select	ENSP00000220616.4:p.Pro2668Ala
ENST00000220616.8:c.8002C>G	ENSP00000220616.4:p.Pro2668Ala
ENST00000519178.5:c.3368C>G
ENST00000519543.5:c.2401C>G	ENSP00000430430.1:p.Pro801Ala
ENST00000521107.1:c.214C>G	ENSP00000430161.1:p.Pro72Ala
ENST00000522691.1:n.88C>G
ENST00000523756.5:c.4657C>G
NM_003235.4:c.8002C>G	NP_003226.4:p.Pro2668Ala
XM_005251038.3:c.7810C>G	XP_005251095.1:p.Pro2604Ala
XM_006716622.2:c.7939C>G	XP_006716685.1:p.Pro2647Ala
XM_005251038.4:c.7810C>G	XP_005251095.1:p.Pro2604Ala
XM_006716622.3:c.7939C>G	XP_006716685.1:p.Pro2647Ala
XM_017013793.1:c.7936C>G	XP_016869282.1:p.Pro2646Ala
XM_017013794.1:c.7867C>G	XP_016869283.1:p.Pro2623Ala
XM_017013795.1:c.7831C>G	XP_016869284.1:p.Pro2611Ala
XM_017013796.1:c.7783C>G	XP_016869285.1:p.Pro2595Ala
XM_017013797.1:c.7741C>G	XP_016869286.1:p.Pro2581Ala
NM_003235.5:c.8002C>G MANE Select	NP_003226.4:p.Pro2668Ala