Linked Data
dbSNP Id:
rs373093471
ExAC:
5:149357949 A / G
gnomAD v2:
5-149357949-A-G
gnomAD v3:
5-149978386-A-G
gnomAD v4:
5-149978386-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149978386A>G , CM000667.2:g.149978386A>G | GRCh38 |
| NC_000005.9:g.149357949A>G , CM000667.1:g.149357949A>G | GRCh37 |
| NC_000005.8:g.149338142A>G | NCBI36 |
| NG_007147.2:g.19504A>G , LRG_684:g.19504A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000690410.1:n.966A>G | ||
| ENST00000286298.5:c.699+35A>G MANE Select | ENSP00000286298.4:n.699+35A>G | |
| ENST00000286298.4:c.699+35A>G | ENSP00000286298.4:n.699+35A>G | |
| ENST00000503336.1:c.372+35A>G | ENSP00000426053.1:n.372+35A>G | |
| NM_000112.3:c.699+35A>G , LRG_684t1:c.699+35A>G | NP_000103.2:n.699+35A>G | |
| XM_017009191.2:c.699+35A>G | XP_016864680.1:n.699+35A>G | |
| NM_000112.4:c.699+35A>G MANE Select | NP_000103.2:n.699+35A>G |