Linked Data
dbSNP Id:
rs570589241
gnomAD v2:
7-135329833-A-G
gnomAD v3:
7-135645085-A-G
gnomAD v4:
7-135645085-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.135645085A>G , CM000669.2:g.135645085A>G | GRCh38 |
| NC_000007.13:g.135329833A>G , CM000669.1:g.135329833A>G | GRCh37 |
| NC_000007.12:g.134980373A>G | NCBI36 |
| NG_051184.1:g.92172A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285968.11:c.5683+67A>G MANE Select | ENSP00000285968.6:n.5683+67A>G | |
| ENST00000285968.10:c.5683+67A>G | ENSP00000285968.6:n.5683+67A>G | |
| ENST00000461255.5:n.890+67A>G | ||
| ENST00000477620.5:c.1405+107A>G | ||
| ENST00000490439.1:c.120+67A>G | ||
| ENST00000607647.5:n.3961+67A>G | ||
| NM_015135.2:c.5683+67A>G | NP_055950.1:n.5683+67A>G | |
| XM_005250235.2:c.4609+67A>G | XP_005250292.1:n.4609+67A>G | |
| NM_001329434.1:c.4609+67A>G | NP_001316363.1:n.4609+67A>G | |
| NM_015135.3:c.5683+67A>G MANE Select | NP_055950.2:n.5683+67A>G | |
| NM_001329434.2:c.4609+67A>G | NP_001316363.2:n.4609+67A>G |