Linked Data
dbSNP Id:
rs16476
gnomAD v2:
7-24330219-T-G
gnomAD v3:
7-24290600-T-G
gnomAD v4:
7-24290600-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.24290600T>G , CM000669.2:g.24290600T>G | GRCh38 |
| NC_000007.13:g.24330219T>G , CM000669.1:g.24330219T>G | GRCh37 |
| NC_000007.12:g.24296744T>G | NCBI36 |
| NG_016148.1:g.11413T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000242152.7:c.269+1021T>G MANE Select | ENSP00000242152.2:n.269+1021T>G | |
| ENST00000242152.6:c.269+1021T>G | ENSP00000242152.2:n.269+1021T>G | |
| ENST00000405982.1:c.269+1021T>G | ENSP00000385282.1:n.269+1021T>G | |
| ENST00000407573.5:c.269+1021T>G | ENSP00000384364.1:n.269+1021T>G | |
| NM_000905.3:c.269+1021T>G | NP_000896.1:n.269+1021T>G | |
| XM_017012910.1:c.41+28757A>C | XP_016868399.1:n.41+28757A>C | |
| XM_017012911.1:c.41+28757A>C | XP_016868400.1:n.41+28757A>C | |
| XR_001745121.1:n.473+28757A>C | ||
| XR_001745122.1:n.345-93571A>C | ||
| XR_001745123.1:n.473+28757A>C | ||
| XR_001745124.1:n.473+28757A>C | ||
| XR_001745125.1:n.473+28757A>C | ||
| XR_001745126.1:n.473+28757A>C | ||
| XR_001745127.1:n.345-34901A>C | ||
| XR_001745129.1:n.473+28757A>C | ||
| XR_001745130.1:n.473+28757A>C | ||
| XR_001745131.1:n.473+28757A>C | ||
| XR_001745132.1:n.473+28757A>C | ||
| NM_000905.4:c.269+1021T>G MANE Select | NP_000896.1:n.269+1021T>G |