Linked Data
dbSNP Id:
rs569559425
gnomAD v2:
12-102164088-G-A
gnomAD v3:
12-101770310-G-A
gnomAD v4:
12-101770310-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.101770310G>A , CM000674.2:g.101770310G>A | GRCh38 |
| NC_000012.11:g.102164088G>A , CM000674.1:g.102164088G>A | GRCh37 |
| NC_000012.10:g.100688219G>A | NCBI36 |
| NG_021243.1:g.65558C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299314.12:c.1113+96C>T MANE Select | ENSP00000299314.7:n.1113+96C>T | |
| ENST00000299314.11:c.1113+96C>T | ENSP00000299314.7:n.1113+96C>T | |
| ENST00000549940.5:c.1113+96C>T | ENSP00000449150.1:n.1113+96C>T | |
| NM_024312.4:c.1113+96C>T | NP_077288.2:n.1113+96C>T | |
| XM_006719593.2:c.1113+96C>T | XP_006719656.1:n.1113+96C>T | |
| XM_011538731.1:c.1032+96C>T | XP_011537033.1:n.1032+96C>T | |
| XM_006719593.3:c.1113+96C>T | XP_006719656.1:n.1113+96C>T | |
| XM_011538731.2:c.1032+96C>T | XP_011537033.1:n.1032+96C>T | |
| XM_017019961.1:c.897+96C>T | XP_016875450.1:n.897+96C>T | |
| XM_017019962.2:c.-115+96C>T | XP_016875451.1:n.-115+96C>T | |
| NM_024312.5:c.1113+96C>T MANE Select | NP_077288.2:n.1113+96C>T |