Canonical Allele Identifier: CA199346547
Gene: TRAF1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.120914118G>T
GRCh37 chr9:g.123676396G>T
gnomAD v2:
9:123676396 G / T
gnomAD v3:
9:120914118 G / T
gnomAD v4:
chr9-120914118-G-T
Joint Max Group AF 0.00004999 (NFE)
Genomes Max Group AF 0.00002849 (NFE)
Exomes Max Group AF 0.00004861 (NFE)
dbSNP:
2416804
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120914118G>T , CM000671.2:g.120914118G>T GRCh38
NC_000009.11:g.123676396G>T , CM000671.1:g.123676396G>T GRCh37
NC_000009.10:g.122716217G>T NCBI36
NG_023346.1:g.20056C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373887.8:c.294+117C>A MANE Select ENSP00000362994.3:n.294+117C>A
ENST00000373887.7:c.294+117C>A ENSP00000362994.3:n.294+117C>A
ENST00000540010.1:c.294+117C>A ENSP00000443183.1:n.294+117C>A
ENST00000546084.5:c.-73+117C>A ENSP00000438583.1:n.-73+117C>A
NM_001190945.1:c.294+117C>A NP_001177874.1:n.294+117C>A
NM_001190947.1:c.-73+117C>A NP_001177876.1:n.-73+117C>A
NM_005658.4:c.294+117C>A NP_005649.1:n.294+117C>A
NM_005658.5:c.294+117C>A MANE Select NP_005649.1:n.294+117C>A
NM_001190945.2:c.294+117C>A NP_001177874.1:n.294+117C>A
NM_001190947.2:c.-73+117C>A NP_001177876.1:n.-73+117C>A
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