Canonical Allele Identifier: CA12999686
Gene: TRAF1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.120911612G>C
GRCh37 chr9:g.123673890G>C
gnomAD v2:
9:123673890 G / C
gnomAD v3:
9:120911612 G / C
gnomAD v4:
chr9-120911612-G-C
Joint Max Group AF 0.32860322 (NFE)
Genomes Max Group AF 0.31679652 (NFE)
Exomes Max Group AF 0.32921174 (NFE)
dbSNP:
7021880
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120911612G>C , CM000671.2:g.120911612G>C GRCh38
NC_000009.11:g.123673890G>C , CM000671.1:g.123673890G>C GRCh37
NC_000009.10:g.122713711G>C NCBI36
NG_023346.1:g.22562C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373887.8:c.706-99C>G MANE Select ENSP00000362994.3:n.706-99C>G
ENST00000373887.7:c.706-99C>G ENSP00000362994.3:n.706-99C>G
ENST00000540010.1:c.706-99C>G ENSP00000443183.1:n.706-99C>G
ENST00000546084.5:c.340-99C>G ENSP00000438583.1:n.340-99C>G
NM_001190945.1:c.706-99C>G NP_001177874.1:n.706-99C>G
NM_001190947.1:c.340-99C>G NP_001177876.1:n.340-99C>G
NM_005658.4:c.706-99C>G NP_005649.1:n.706-99C>G
NM_005658.5:c.706-99C>G MANE Select NP_005649.1:n.706-99C>G
NM_001190945.2:c.706-99C>G NP_001177874.1:n.706-99C>G
NM_001190947.2:c.340-99C>G NP_001177876.1:n.340-99C>G
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