Canonical Allele Identifier: CA12999700
Gene: TRAF1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.120923941C>G
GRCh37 chr9:g.123686219C>G
gnomAD v2:
9:123686219 C / G
gnomAD v3:
9:120923941 C / G
gnomAD v4:
chr9-120923941-C-G
Joint Max Group AF 0.81574172 (SAS)
Genomes Max Group AF 0.79637594 (SAS)
Exomes Max Group AF 0.81583805 (SAS)
dbSNP:
1930780
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120923941C>G , CM000671.2:g.120923941C>G GRCh38
NC_000009.11:g.123686219C>G , CM000671.1:g.123686219C>G GRCh37
NC_000009.10:g.122726040C>G NCBI36
NG_023346.1:g.10233G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373887.8:c.141-149G>C MANE Select ENSP00000362994.3:n.141-149G>C
ENST00000373887.7:c.141-149G>C ENSP00000362994.3:n.141-149G>C
ENST00000540010.1:c.141-149G>C ENSP00000443183.1:n.141-149G>C
NM_001190945.1:c.141-149G>C NP_001177874.1:n.141-149G>C
NM_005658.4:c.141-149G>C NP_005649.1:n.141-149G>C
NM_005658.5:c.141-149G>C MANE Select NP_005649.1:n.141-149G>C
NM_001190945.2:c.141-149G>C NP_001177874.1:n.141-149G>C
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