Linked Data
ClinVar Variation Id:
926025
dbSNP Id:
rs368462984
ExAC:
15:67358687 C / T
gnomAD v2:
15-67358687-C-T
gnomAD v3:
15-67066349-C-T
gnomAD v4:
15-67066349-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.67066349C>T , CM000677.2:g.67066349C>T | GRCh38 |
| NC_000015.9:g.67358687C>T , CM000677.1:g.67358687C>T | GRCh37 |
| NC_000015.8:g.65145741C>T | NCBI36 |
| NG_011990.1:g.5493C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559460.6:c.-110+2405C>T | ENSP00000453082.2:n.-110+2405C>T | |
| ENST00000560424.2:c.195C>T | ENSP00000455540.2:p.Ile65= | |
| ENST00000327367.9:c.195C>T MANE Select | ENSP00000332973.4:p.Ile65= | |
| ENST00000327367.8:c.195C>T | ENSP00000332973.4:p.Ile65= | |
| ENST00000559460.5:c.-110+2405C>T | ENSP00000453082.1:n.-110+2405C>T | |
| NM_005902.3:c.195C>T | NP_005893.1:p.Ile65= | |
| XM_011521559.1:c.195C>T | XP_011519861.1:p.Ile65= | |
| XM_011521559.3:c.195C>T | XP_011519861.1:p.Ile65= | |
| NM_005902.4:c.195C>T MANE Select | NP_005893.1:p.Ile65= |