Linked Data
dbSNP Id:
rs17408276
gnomAD v2:
15-78881618-T-C
gnomAD v3:
15-78589276-T-C
gnomAD v4:
15-78589276-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.78589276T>C , CM000677.2:g.78589276T>C | GRCh38 |
| NC_000015.9:g.78881618T>C , CM000677.1:g.78881618T>C | GRCh37 |
| NC_000015.8:g.76668673T>C | NCBI36 |
| NG_023328.1:g.28757T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000299565.9:c.414-529T>C MANE Select | ENSP00000299565.5:n.414-529T>C | |
| ENST00000394802.4:c.229-529T>C | ||
| ENST00000559554.5:c.414-529T>C | ENSP00000453519.1:n.414-529T>C | |
| NM_000745.3:c.414-529T>C | NP_000736.2:n.414-529T>C | |
| NM_001307945.1:c.414-529T>C | NP_001294874.1:n.414-529T>C | |
| XM_005254142.2:c.414-529T>C | XP_005254199.1:n.414-529T>C | |
| NM_001307945.2:c.414-529T>C | NP_001294874.1:n.414-529T>C | |
| NM_000745.4:c.414-529T>C MANE Select | NP_000736.2:n.414-529T>C | |
| NM_001395171.1:c.414-529T>C | NP_001382100.1:n.414-529T>C | |
| NM_001395172.1:c.414-529T>C | NP_001382101.1:n.414-529T>C | |
| NM_001395173.1:c.414-529T>C | NP_001382102.1:n.414-529T>C | |
| NM_001395174.1:c.414-529T>C | NP_001382103.1:n.414-529T>C | |
| NM_001395175.1:c.411-529T>C | NP_001382104.1:n.411-529T>C |