Canonical Allele Identifier: CA10658701
Gene: TNFRSF9 HGNC NCBI
COSMIC:
COSN6469193 (not active)
MyVariant.info:
GRCh38 chr1:g.7929506C>T
GRCh37 chr1:g.7989566C>T
gnomAD v2:
1:7989566 C / T
gnomAD v3:
1:7929506 C / T
gnomAD v4:
chr1-7929506-C-T
Joint Max Group AF 0.46271977 (MID)
Genomes Max Group AF 0.40057168 (SAS)
dbSNP:
2453021
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.7929506C>T , CM000663.2:g.7929506C>T GRCh38
NC_000001.10:g.7989566C>T , CM000663.1:g.7989566C>T GRCh37
NC_000001.9:g.7912153C>T NCBI36
NG_052834.1:g.18660G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377507.8:c.679+3656G>A MANE Select ENSP00000366729.3:n.679+3656G>A
ENST00000377507.7:c.679+3656G>A ENSP00000366729.3:n.679+3656G>A
ENST00000474475.1:c.223+3656G>A ENSP00000465272.1:n.223+3656G>A
ENST00000615230.4:c.679+3656G>A ENSP00000478699.1:n.679+3656G>A
NM_001561.5:c.679+3656G>A NP_001552.2:n.679+3656G>A
XM_006710618.2:c.679+3656G>A XP_006710681.1:n.679+3656G>A
XM_011541386.1:c.679+3656G>A XP_011539688.1:n.679+3656G>A
XM_006710618.3:c.679+3656G>A XP_006710681.1:n.679+3656G>A
XM_011541386.2:c.679+3656G>A XP_011539688.1:n.679+3656G>A
NM_001561.6:c.679+3656G>A MANE Select NP_001552.2:n.679+3656G>A
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