Linked Data
ClinVar Variation Id:
2952426
ClinVar RCV Id:
RCV003815577
dbSNP Id:
rs1042977592
gnomAD v2:
2-167060856-A-G
gnomAD v4:
2-166204346-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.166204346A>G , CM000664.2:g.166204346A>G | GRCh38 |
| NC_000002.11:g.167060856A>G , CM000664.1:g.167060856A>G | GRCh37 |
| NC_000002.10:g.166769102A>G | NCBI36 |
| NG_012798.1:g.176642T>C , LRG_369:g.176642T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303354.11:c.4503+14T>C (SCN9A) | ENSP00000304748.7:n.4503+14T>C | |
| ENST00000409435.6:c.4503+14T>C (SCN9A) | ENSP00000386330.2:n.4503+14T>C | |
| ENST00000642356.2:c.4503+14T>C (SCN9A) MANE Select | ENSP00000495601.1:n.4503+14T>C | |
| ENST00000644316.1:c.4347+14T>C (SCN9A) | ENSP00000493939.1:n.4347+14T>C | |
| ENST00000645907.1:c.4470+14T>C (SCN9A) | ENSP00000495983.1:n.4470+14T>C | |
| ENST00000646694.1:n.880+14T>C (SCN9A) | ||
| ENST00000303354.10:c.4503+14T>C (SCN9A) | ENSP00000304748.7:n.4503+14T>C | |
| ENST00000409435.5:c.4503+14T>C (SCN9A) | ENSP00000386330.1:n.4503+14T>C | |
| ENST00000409672.5:c.4470+14T>C (SCN9A) | ENSP00000386306.1:n.4470+14T>C | |
| NM_002977.3:c.4470+14T>C , LRG_369t1:c.4470+14T>C (SCN9A) | NP_002968.1:n.4470+14T>C | |
| NR_110260.1:n.611+4528A>G (SCN1A-AS1) | ||
| XM_005246757.1:c.4503+14T>C (SCN9A) | XP_005246814.1:n.4503+14T>C | |
| XM_011511616.1:c.4503+14T>C (SCN9A) | XP_011509918.1:n.4503+14T>C | |
| XM_011511617.1:c.4503+14T>C (SCN9A) | XP_011509919.1:n.4503+14T>C | |
| XM_011511618.1:c.4470+14T>C (SCN9A) | XP_011509920.1:n.4470+14T>C | |
| XM_011511619.1:c.4503+14T>C (SCN9A) | XP_011509921.1:n.4503+14T>C | |
| NM_001365536.1:c.4503+14T>C (SCN9A) MANE Select | NP_001352465.1:n.4503+14T>C | |
| XM_011511616.3:c.4503+14T>C (SCN9A) | XP_011509918.1:n.4503+14T>C | |
| XM_011511617.2:c.4503+14T>C (SCN9A) | XP_011509919.1:n.4503+14T>C | |
| XM_011511618.2:c.4470+14T>C (SCN9A) | XP_011509920.1:n.4470+14T>C | |
| XM_011511619.2:c.4503+14T>C (SCN9A) | XP_011509921.1:n.4503+14T>C | |
| XM_017004668.1:c.4116+14T>C (SCN9A) | XP_016860157.1:n.4116+14T>C | |
| XM_017004669.1:c.3759+14T>C (SCN9A) | XP_016860158.1:n.3759+14T>C |