Linked Data
dbSNP Id:
rs756589255
ExAC:
16:4812597 C / A
gnomAD v2:
16-4812597-C-A
gnomAD v3:
16-4762596-C-A
gnomAD v4:
16-4762596-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.4762596C>A , CM000678.2:g.4762596C>A | GRCh38 |
| NC_000016.9:g.4812597C>A , CM000678.1:g.4812597C>A | GRCh37 |
| NC_000016.8:g.4752598C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000219478.11:c.575G>T MANE Select | ENSP00000219478.5:p.Gly192Val | |
| ENST00000219478.10:c.575G>T | ENSP00000219478.5:p.Gly192Val | |
| ENST00000545009.1:c.575G>T | ENSP00000445714.1:p.Gly192Val | |
| ENST00000589422.1:c.*103G>T | ENSP00000466375.1:n.*103G>T | |
| NM_001303450.1:c.575G>T | NP_001290379.1:p.Gly192Val | |
| NM_021646.2:c.575G>T | NP_067678.1:p.Gly192Val | |
| XM_005255243.2:c.224G>T | XP_005255300.1:p.Gly75Val | |
| XM_011522453.1:c.575G>T | XP_011520755.1:p.Gly192Val | |
| XM_011522454.1:c.-50G>T | XP_011520756.1:n.-50G>T | |
| NM_021646.3:c.575G>T | NP_067678.1:p.Gly192Val | |
| XM_005255243.4:c.224G>T | XP_005255300.1:p.Gly75Val | |
| XM_011522453.2:c.575G>T | XP_011520755.1:p.Gly192Val | |
| XM_011522454.3:c.-50G>T | XP_011520756.1:n.-50G>T | |
| XM_017023121.2:c.-50G>T | XP_016878610.1:n.-50G>T | |
| NM_001303450.2:c.575G>T | NP_001290379.1:p.Gly192Val | |
| NM_021646.4:c.575G>T MANE Select | NP_067678.1:p.Gly192Val |