Linked Data
ClinVar Variation Id:
558175
dbSNP Id:
rs1215582852
gnomAD v2:
17-40695796-T-C
gnomAD v3:
17-42543778-T-C
gnomAD v4:
17-42543778-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42543778T>C , CM000679.2:g.42543778T>C | GRCh38 |
| NC_000017.10:g.40695796T>C , CM000679.1:g.40695796T>C | GRCh37 |
| NC_000017.9:g.37949322T>C | NCBI36 |
| NG_011552.1:g.12846T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.1772T>C MANE Select | ENSP00000225927.1:p.Leu591Pro | |
| ENST00000225927.6:c.1772T>C | ENSP00000225927.1:p.Leu591Pro | |
| ENST00000591587.1:c.1110T>C | ENSP00000467836.1:n.1110T>C | |
| NM_000263.3:c.1772T>C | NP_000254.2:p.Leu591Pro | |
| XM_006721920.2:c.941T>C | XP_006721983.1:p.Leu314Pro | |
| XM_011524840.1:c.773T>C | XP_011523142.1:p.Leu258Pro | |
| XM_017024687.1:c.941T>C | XP_016880176.1:p.Leu314Pro | |
| XM_024450771.1:c.1829T>C | XP_024306539.1:p.Leu610Pro | |
| XM_024450772.1:c.773T>C | XP_024306540.1:p.Leu258Pro | |
| NM_000263.4:c.1772T>C MANE Select | NP_000254.2:p.Leu591Pro |