Linked Data
ClinVar Variation Id:
1667956
ClinVar RCV Id:
RCV002191493
dbSNP Id:
rs1558945498
gnomAD v2:
2-167060860-A-T
gnomAD v3:
2-166204350-A-T
gnomAD v4:
2-166204350-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.166204350A>T , CM000664.2:g.166204350A>T | GRCh38 |
| NC_000002.11:g.167060860A>T , CM000664.1:g.167060860A>T | GRCh37 |
| NC_000002.10:g.166769106A>T | NCBI36 |
| NG_012798.1:g.176638T>A , LRG_369:g.176638T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303354.11:c.4503+10T>A (SCN9A) | ENSP00000304748.7:n.4503+10T>A | |
| ENST00000409435.6:c.4503+10T>A (SCN9A) | ENSP00000386330.2:n.4503+10T>A | |
| ENST00000642356.2:c.4503+10T>A (SCN9A) MANE Select | ENSP00000495601.1:n.4503+10T>A | |
| ENST00000644316.1:c.4347+10T>A (SCN9A) | ENSP00000493939.1:n.4347+10T>A | |
| ENST00000645907.1:c.4470+10T>A (SCN9A) | ENSP00000495983.1:n.4470+10T>A | |
| ENST00000646694.1:n.880+10T>A (SCN9A) | ||
| ENST00000303354.10:c.4503+10T>A (SCN9A) | ENSP00000304748.7:n.4503+10T>A | |
| ENST00000409435.5:c.4503+10T>A (SCN9A) | ENSP00000386330.1:n.4503+10T>A | |
| ENST00000409672.5:c.4470+10T>A (SCN9A) | ENSP00000386306.1:n.4470+10T>A | |
| NM_002977.3:c.4470+10T>A , LRG_369t1:c.4470+10T>A (SCN9A) | NP_002968.1:n.4470+10T>A | |
| NR_110260.1:n.611+4532A>T (SCN1A-AS1) | ||
| XM_005246757.1:c.4503+10T>A (SCN9A) | XP_005246814.1:n.4503+10T>A | |
| XM_011511616.1:c.4503+10T>A (SCN9A) | XP_011509918.1:n.4503+10T>A | |
| XM_011511617.1:c.4503+10T>A (SCN9A) | XP_011509919.1:n.4503+10T>A | |
| XM_011511618.1:c.4470+10T>A (SCN9A) | XP_011509920.1:n.4470+10T>A | |
| XM_011511619.1:c.4503+10T>A (SCN9A) | XP_011509921.1:n.4503+10T>A | |
| NM_001365536.1:c.4503+10T>A (SCN9A) MANE Select | NP_001352465.1:n.4503+10T>A | |
| XM_011511616.3:c.4503+10T>A (SCN9A) | XP_011509918.1:n.4503+10T>A | |
| XM_011511617.2:c.4503+10T>A (SCN9A) | XP_011509919.1:n.4503+10T>A | |
| XM_011511618.2:c.4470+10T>A (SCN9A) | XP_011509920.1:n.4470+10T>A | |
| XM_011511619.2:c.4503+10T>A (SCN9A) | XP_011509921.1:n.4503+10T>A | |
| XM_017004668.1:c.4116+10T>A (SCN9A) | XP_016860157.1:n.4116+10T>A | |
| XM_017004669.1:c.3759+10T>A (SCN9A) | XP_016860158.1:n.3759+10T>A |