Linked Data
ClinVar Variation Id:
48361
dbSNP Id:
rs145207584
ExAC:
1:215953266 T / C
gnomAD v2:
1-215953266-T-C
gnomAD v3:
1-215779924-T-C
gnomAD v4:
1-215779924-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215779924T>C , CM000663.2:g.215779924T>C | GRCh38 |
| NC_000001.10:g.215953266T>C , CM000663.1:g.215953266T>C | GRCh37 |
| NC_000001.9:g.214019889T>C | NCBI36 |
| NG_009497.1:g.648473A>G | |
| NG_009497.2:g.648525A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307340.8:c.10858A>G MANE Select | ENSP00000305941.3:p.Ile3620Val | |
| ENST00000674083.1:c.10858A>G | ENSP00000501296.1:p.Ile3620Val | |
| ENST00000307340.7:c.10858A>G | ENSP00000305941.3:p.Ile3620Val | |
| NM_206933.2:c.10858A>G | NP_996816.2:p.Ile3620Val | |
| NM_206933.3:c.10858A>G | NP_996816.2:p.Ile3620Val | |
| NM_206933.4:c.10858A>G MANE Select | NP_996816.3:p.Ile3620Val |