Linked Data
ClinVar Variation Id:
2507270
ClinVar RCV Id:
RCV003239161
dbSNP Id:
rs146437238
gnomAD v2:
9-140093905-G-C
gnomAD v4:
9-137199453-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137199453G>C , CM000671.2:g.137199453G>C | GRCh38 |
| NC_000009.11:g.140093905G>C , CM000671.1:g.140093905G>C | GRCh37 |
| NC_000009.10:g.139213726G>C | NCBI36 |
| NG_027801.1:g.6259C>G | |
| NG_027801.2:g.9741C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409012.6:c.1259C>G MANE Select | ENSP00000387100.4:p.Pro420Arg | |
| ENST00000333046.8:c.653C>G | ENSP00000327617.4:p.Pro218Arg | |
| ENST00000409012.4:c.1259C>G | ENSP00000387100.4:p.Pro420Arg | |
| ENST00000541945.1:n.90+4651C>G | ||
| NM_001128228.2:c.1259C>G | NP_001121700.2:p.Pro420Arg | |
| NM_001128228.3:c.1259C>G MANE Select | NP_001121700.2:p.Pro420Arg |