Linked Data
dbSNP Id:
rs1244410065
gnomAD v2:
16-1560960-T-C
gnomAD v3:
16-1510959-T-C
gnomAD v4:
16-1510959-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1510959T>C , CM000678.2:g.1510959T>C | GRCh38 |
| NC_000016.9:g.1560960T>C , CM000678.1:g.1560960T>C | GRCh37 |
| NC_000016.8:g.1500961T>C | NCBI36 |
| NG_032783.1:g.106150A>G | |
| NG_050910.1:g.22616T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000426508.7:c.4374A>G MANE Select | ENSP00000406012.2:p.Ala1458= | |
| ENST00000361339.9:c.1956A>G | ENSP00000354895.5:p.Ala652= | |
| ENST00000397417.6:c.*2812A>G | ENSP00000380562.2:n.*2812A>G | |
| ENST00000426508.6:c.4374A>G | ENSP00000406012.2:p.Ala1458= | |
| ENST00000565298.5:n.4198A>G | ||
| NM_014714.3:c.4374A>G | NP_055529.2:p.Ala1458= | |
| XM_006720989.2:c.4374A>G | XP_006721052.1:p.Ala1458= | |
| XM_006720990.2:c.4374A>G | XP_006721053.1:p.Ala1458= | |
| XM_006720991.2:c.4374A>G | XP_006721054.1:p.Ala1458= | |
| XM_006720992.2:c.2007A>G | XP_006721055.1:p.Ala669= | |
| XM_011522766.1:c.4128A>G | XP_011521068.1:p.Ala1376= | |
| XM_011522767.1:c.3399A>G | XP_011521069.1:p.Ala1133= | |
| XM_006720990.3:c.4374A>G | XP_006721053.1:p.Ala1458= | |
| XM_006720991.3:c.4374A>G | XP_006721054.1:p.Ala1458= | |
| XM_006720992.3:c.2007A>G | XP_006721055.1:p.Ala669= | |
| XM_011522766.3:c.4128A>G | XP_011521068.1:p.Ala1376= | |
| XM_011522767.2:c.3399A>G | XP_011521069.1:p.Ala1133= | |
| XM_017023910.1:c.4374A>G | XP_016879399.1:p.Ala1458= | |
| XM_017023911.1:c.2559A>G | XP_016879400.1:p.Ala853= | |
| NM_014714.4:c.4374A>G MANE Select | NP_055529.2:p.Ala1458= |