Canonical Allele Identifier: CA363318479

Gene: TCF19

Linked Data

• dbSNP Id: rs1229454831
• MyVariant Identifiers: chr6:g.31129781G>A (hg19) ; chr6:g.31162004G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31162004G>A , CM000668.2:g.31162004G>A	GRCh38
NC_000006.11:g.31129781G>A , CM000668.1:g.31129781G>A	GRCh37
NC_000006.10:g.31237760G>A	NCBI36
NG_054878.1:g.1235C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542218.2:c.796G>A	ENSP00000439397.2:p.Gly266Arg
ENST00000706778.1:c.796G>A	ENSP00000516543.1:p.Gly266Arg
ENST00000706779.1:c.796G>A	ENSP00000516544.1:p.Gly266Arg
ENST00000706780.1:c.796G>A	ENSP00000516545.1:p.Gly266Arg
ENST00000706781.1:c.796G>A	ENSP00000516546.1:p.Gly266Arg
ENST00000706782.1:c.796G>A	ENSP00000516547.1:p.Gly266Arg
ENST00000706783.1:c.*24G>A	ENSP00000516548.1:n.*24G>A
ENST00000706785.1:c.*89G>A	ENSP00000516549.1:n.*89G>A
ENST00000706786.1:c.*24G>A	ENSP00000516550.1:n.*24G>A
ENST00000706787.1:c.796G>A	ENSP00000516551.1:p.Gly266Arg
ENST00000706788.1:n.747G>A
ENST00000376257.8:c.796G>A MANE Select	ENSP00000365433.3:p.Gly266Arg
ENST00000376255.4:c.796G>A	ENSP00000365431.4:p.Gly266Arg
ENST00000376257.7:c.796G>A	ENSP00000365433.3:p.Gly266Arg
ENST00000496421.1:n.348G>A
ENST00000542218.1:c.556G>A	ENSP00000439397.1:p.Gly186Arg
NM_001077511.1:c.796G>A	NP_001070979.1:p.Gly266Arg
NM_007109.2:c.796G>A	NP_009040.2:p.Gly266Arg
XM_005249334.2:c.796G>A	XP_005249391.1:p.Gly266Arg
XM_011514829.1:c.796G>A	XP_011513131.1:p.Gly266Arg
NM_001318908.1:c.796G>A	NP_001305837.1:p.Gly266Arg
NM_007109.3:c.796G>A MANE Select	NP_009040.2:p.Gly266Arg
NM_001077511.2:c.796G>A	NP_001070979.1:p.Gly266Arg
NM_001318908.2:c.796G>A	NP_001305837.1:p.Gly266Arg