Canonical Allele Identifier: CA15434236
Gene: TCF19 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.31162816G>A
GRCh37 chr6:g.31130593G>A
gnomAD v2:
6:31130593 G / A
gnomAD v3:
6:31162816 G / A
gnomAD v4:
chr6-31162816-G-A
Joint Max Group AF 0.61256061 (AFR)
Genomes Max Group AF 0.60925437 (AFR)
Exomes Max Group AF 0.61238694 (AFR)
dbSNP:
1419881
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31162816G>A , CM000668.2:g.31162816G>A GRCh38
NC_000006.11:g.31130593G>A , CM000668.1:g.31130593G>A GRCh37
NC_000006.10:g.31238572G>A NCBI36
NG_054878.1:g.423C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000542218.2:c.797+811G>A ENSP00000439397.2:n.797+811G>A
ENST00000706778.1:c.*99G>A ENSP00000516543.1:n.*99G>A
ENST00000706779.1:c.*99G>A ENSP00000516544.1:n.*99G>A
ENST00000706780.1:c.*99G>A ENSP00000516545.1:n.*99G>A
ENST00000706781.1:c.*99G>A ENSP00000516546.1:n.*99G>A
ENST00000706782.1:c.798-1G>A ENSP00000516547.1:n.798-1G>A
ENST00000706783.1:c.*365G>A ENSP00000516548.1:n.*365G>A
ENST00000706785.1:c.*430G>A ENSP00000516549.1:n.*430G>A
ENST00000706786.1:c.*365G>A ENSP00000516550.1:n.*365G>A
ENST00000706787.1:c.*99G>A ENSP00000516551.1:n.*99G>A
ENST00000706788.1:n.1088G>A
ENST00000376257.8:c.*99G>A MANE Select ENSP00000365433.3:n.*99G>A
ENST00000376255.4:c.*99G>A ENSP00000365431.4:n.*99G>A
ENST00000376257.7:c.*99G>A ENSP00000365433.3:n.*99G>A
ENST00000496421.1:n.689G>A
ENST00000542218.1:c.557+811G>A ENSP00000439397.1:n.557+811G>A
NM_001077511.1:c.*99G>A NP_001070979.1:n.*99G>A
NM_007109.2:c.*99G>A NP_009040.2:n.*99G>A
XM_005249334.2:c.*99G>A XP_005249391.1:n.*99G>A
XM_011514829.1:c.*99G>A XP_011513131.1:n.*99G>A
NM_001318908.1:c.*99G>A NP_001305837.1:n.*99G>A
NM_007109.3:c.*99G>A MANE Select NP_009040.2:n.*99G>A
NM_001077511.2:c.*99G>A NP_001070979.1:n.*99G>A
NM_001318908.2:c.*99G>A NP_001305837.1:n.*99G>A
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