Linked Data
dbSNP Id:
rs779284269
ExAC:
17:27838032 C / T
gnomAD v2:
17-27838032-C-T
gnomAD v4:
17-29511014-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.29511014C>T , CM000679.2:g.29511014C>T | GRCh38 |
| NC_000017.10:g.27838032C>T , CM000679.1:g.27838032C>T | GRCh37 |
| NC_000017.9:g.24862158C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261716.8:c.1704+22C>T MANE Select | ENSP00000261716.3:n.1704+22C>T | |
| ENST00000261716.7:c.1704+22C>T | ENSP00000261716.3:n.1704+22C>T | |
| ENST00000536202.1:c.1704+22C>T | ENSP00000438819.1:n.1704+22C>T | |
| ENST00000577583.1:n.1574C>T | ||
| NM_020791.2:c.1704+22C>T | NP_065842.1:n.1704+22C>T | |
| NM_025142.1:c.1704+22C>T | NP_079418.1:n.1704+22C>T | |
| XM_011525060.1:c.1704+22C>T | XP_011523362.1:n.1704+22C>T | |
| XM_011525060.2:c.1704+22C>T | XP_011523362.1:n.1704+22C>T | |
| NM_020791.4:c.1704+22C>T MANE Select | NP_065842.1:n.1704+22C>T |