Linked Data
dbSNP Id:
rs770870064
gnomAD v4:
16-3729149-G-C
MyVariant Identifiers:
chr16:g.3779150G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3729149G>C , CM000678.2:g.3729149G>C | GRCh38 |
| NC_000016.9:g.3779150G>C , CM000678.1:g.3779150G>C | GRCh37 |
| NC_000016.8:g.3719151G>C | NCBI36 |
| NG_009873.1:g.155972C>G | |
| NG_009873.2:g.156565C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262367.10:c.5898C>G MANE Select | ENSP00000262367.5:p.Ala1966= | |
| ENST00000262367.9:c.5898C>G | ENSP00000262367.5:p.Ala1966= | |
| ENST00000382070.7:c.5784C>G | ENSP00000371502.3:p.Ala1928= | |
| NM_001079846.1:c.5784C>G | NP_001073315.1:p.Ala1928= | |
| NM_004380.2:c.5898C>G | NP_004371.2:p.Ala1966= | |
| XM_005255124.3:c.5853C>G | XP_005255181.1:p.Ala1951= | |
| XM_005255125.3:c.5481C>G | XP_005255182.1:p.Ala1827= | |
| XM_006720848.2:c.5637C>G | XP_006720911.1:p.Ala1879= | |
| XM_011522380.1:c.5844C>G | XP_011520682.1:p.Ala1948= | |
| XM_011522381.1:c.5145C>G | XP_011520683.1:p.Ala1715= | |
| XM_005255124.4:c.5853C>G | XP_005255181.1:p.Ala1951= | |
| XM_005255125.4:c.5481C>G | XP_005255182.1:p.Ala1827= | |
| XM_006720848.3:c.5637C>G | XP_006720911.1:p.Ala1879= | |
| XM_011522381.2:c.5145C>G | XP_011520683.1:p.Ala1715= | |
| XM_017022944.1:c.5892C>G | XP_016878433.1:p.Ala1964= | |
| NM_004380.3:c.5898C>G MANE Select | NP_004371.2:p.Ala1966= |