Linked Data
dbSNP Id:
rs762523931
ExAC:
17:4535248 T / C
gnomAD v2:
17-4535248-T-C
gnomAD v3:
17-4631953-T-C
gnomAD v4:
17-4631953-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4631953T>C , CM000679.2:g.4631953T>C | GRCh38 |
| NC_000017.10:g.4535248T>C , CM000679.1:g.4535248T>C | GRCh37 |
| NC_000017.9:g.4481997T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293761.8:c.1745A>G MANE Select | ENSP00000293761.3:p.Asn582Ser | |
| ENST00000570836.6:c.1745A>G | ENSP00000458832.1:p.Asn582Ser | |
| ENST00000293761.7:c.1745A>G | ENSP00000293761.3:p.Asn582Ser | |
| ENST00000570836.5:c.1745A>G | ENSP00000458832.1:p.Asn582Ser | |
| ENST00000574640.1:c.1628A>G | ENSP00000460483.1:p.Asn543Ser | |
| NM_001140.3:c.1745A>G | NP_001131.3:p.Asn582Ser | |
| NM_001140.4:c.1745A>G | NP_001131.3:p.Asn582Ser | |
| NM_001140.5:c.1745A>G MANE Select | NP_001131.3:p.Asn582Ser |