Linked Data
ClinVar Variation Id:
2057053
ClinVar RCV Id:
RCV002923156
dbSNP Id:
rs1266960517
gnomAD v2:
7-143018957-C-G
gnomAD v4:
7-143321864-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.143321864C>G , CM000669.2:g.143321864C>G | GRCh38 |
| NC_000007.13:g.143018957C>G , CM000669.1:g.143018957C>G | GRCh37 |
| NC_000007.12:g.142729079C>G | NCBI36 |
| NG_009815.1:g.10739C>G | |
| NG_009815.2:g.10739C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650516.2:c.696+16C>G | ENSP00000498052.2:n.696+16C>G | |
| ENST00000343257.7:c.696+16C>G MANE Select | ENSP00000339867.2:n.696+16C>G | |
| ENST00000432192.6:c.464+16C>G | ||
| ENST00000455478.6:c.150+16C>G | ENSP00000400027.2:n.150+16C>G | |
| ENST00000650516.1:c.696+16C>G | ENSP00000498052.1:n.696+16C>G | |
| ENST00000343257.6:c.696+16C>G | ENSP00000339867.2:n.696+16C>G | |
| ENST00000432192.5:c.154+16C>G | ||
| ENST00000455478.5:c.154+16C>G | ||
| ENST00000495612.1:n.154+16C>G | ||
| NM_000083.2:c.696+16C>G | NP_000074.2:n.696+16C>G | |
| NR_046453.1:n.783+16C>G | ||
| XM_011515781.1:c.696+16C>G | XP_011514083.1:n.696+16C>G | |
| XM_017011739.1:c.403+16C>G | XP_016867228.1:n.403+16C>G | |
| XM_017011740.1:c.403+16C>G | XP_016867229.1:n.403+16C>G | |
| NM_000083.3:c.696+16C>G MANE Select | NP_000074.3:n.696+16C>G | |
| NR_046453.2:n.798+16C>G |