Linked Data
ClinVar Variation Id:
453305
ClinVar RCV Id:
RCV000549562
dbSNP Id:
rs1386720703
gnomAD v4:
20-4699400-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.4699400T>C , CM000682.2:g.4699400T>C | GRCh38 |
| NC_000020.10:g.4680046T>C , CM000682.1:g.4680046T>C | GRCh37 |
| NC_000020.9:g.4628046T>C | NCBI36 |
| NG_009087.1:g.18250T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379440.9:c.180T>C MANE Select | ENSP00000368752.4:p.Pro60= | |
| ENST00000424424.2:c.180T>C | ENSP00000411599.2:p.Pro60= | |
| ENST00000457586.2:c.180T>C | ENSP00000415284.2:p.Pro60= | |
| ENST00000379440.8:c.180T>C | ENSP00000368752.4:p.Pro60= | |
| ENST00000424424.1:c.180T>C | ENSP00000411599.1:p.Pro60= | |
| ENST00000430350.2:c.180T>C | ENSP00000399376.2:p.Pro60= | |
| ENST00000457586.1:c.180T>C | ENSP00000415284.1:p.Pro60= | |
| NM_000311.3:c.180T>C | NP_000302.1:p.Pro60= | |
| NM_001080121.1:c.180T>C | NP_001073590.1:p.Pro60= | |
| NM_001080122.1:c.180T>C | NP_001073591.1:p.Pro60= | |
| NM_001080123.1:c.180T>C | NP_001073592.1:p.Pro60= | |
| NM_001271561.1:c.91T>C | NP_001258490.1:p.Ser31Pro | |
| NM_183079.2:c.180T>C | NP_898902.1:p.Pro60= | |
| NM_000311.4:c.180T>C | NP_000302.1:p.Pro60= | |
| NM_001080121.2:c.180T>C | NP_001073590.1:p.Pro60= | |
| NM_001080122.2:c.180T>C | NP_001073591.1:p.Pro60= | |
| NM_001080123.2:c.180T>C | NP_001073592.1:p.Pro60= | |
| NM_001271561.2:c.91T>C | NP_001258490.1:p.Ser31Pro | |
| NM_183079.3:c.180T>C | NP_898902.1:p.Pro60= | |
| NM_000311.5:c.180T>C MANE Select | NP_000302.1:p.Pro60= | |
| NM_001080121.3:c.180T>C | NP_001073590.1:p.Pro60= | |
| NM_001080122.3:c.180T>C | NP_001073591.1:p.Pro60= | |
| NM_001080123.3:c.180T>C | NP_001073592.1:p.Pro60= | |
| NM_001271561.3:c.91T>C | NP_001258490.1:p.Ser31Pro | |
| NM_183079.4:c.180T>C | NP_898902.1:p.Pro60= |