Linked Data
dbSNP Id:
rs981921576
gnomAD v2:
11-8111575-T-C
gnomAD v3:
11-8090028-T-C
gnomAD v4:
11-8090028-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.8090028T>C , CM000673.2:g.8090028T>C | GRCh38 |
| NC_000011.9:g.8111575T>C , CM000673.1:g.8111575T>C | GRCh37 |
| NC_000011.8:g.8068151T>C | NCBI36 |
| NG_029912.1:g.56396T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000299506.3:c.91-41T>C MANE Select | ENSP00000299506.3:n.91-41T>C | |
| ENST00000299506.2:c.91-41T>C | ENSP00000299506.2:n.91-41T>C | |
| ENST00000305253.8:c.256-41T>C | ENSP00000305426.4:n.256-41T>C | |
| ENST00000534099.5:c.109-41T>C | ENSP00000434400.1:n.109-41T>C | |
| NM_003320.4:c.256-41T>C | NP_003311.2:n.256-41T>C | |
| NM_177972.2:c.91-41T>C | NP_813977.1:n.91-41T>C | |
| XM_005253109.2:c.217-41T>C | XP_005253166.1:n.217-41T>C | |
| XM_011520344.1:c.127-41T>C | XP_011518646.1:n.127-41T>C | |
| XM_005253109.3:c.217-41T>C | XP_005253166.1:n.217-41T>C | |
| XM_011520344.2:c.127-41T>C | XP_011518646.1:n.127-41T>C | |
| NM_177972.3:c.91-41T>C MANE Select | NP_813977.1:n.91-41T>C | |
| NM_003320.5:c.256-41T>C | NP_003311.2:n.256-41T>C |