Linked Data
dbSNP Id:
rs377692518
gnomAD v4:
16-3728036-C-A
MyVariant Identifiers:
chr16:g.3778037C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3728036C>A , CM000678.2:g.3728036C>A | GRCh38 |
| NC_000016.9:g.3778037C>A , CM000678.1:g.3778037C>A | GRCh37 |
| NC_000016.8:g.3718038C>A | NCBI36 |
| NG_009873.1:g.157085G>T | |
| NG_009873.2:g.157678G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262367.10:c.7011G>T MANE Select | ENSP00000262367.5:p.Thr2337= | |
| ENST00000262367.9:c.7011G>T | ENSP00000262367.5:p.Thr2337= | |
| ENST00000382070.7:c.6897G>T | ENSP00000371502.3:p.Thr2299= | |
| NM_001079846.1:c.6897G>T | NP_001073315.1:p.Thr2299= | |
| NM_004380.2:c.7011G>T | NP_004371.2:p.Thr2337= | |
| XM_005255124.3:c.6966G>T | XP_005255181.1:p.Thr2322= | |
| XM_005255125.3:c.6594G>T | XP_005255182.1:p.Thr2198= | |
| XM_006720848.2:c.6750G>T | XP_006720911.1:p.Thr2250= | |
| XM_011522380.1:c.6957G>T | XP_011520682.1:p.Thr2319= | |
| XM_011522381.1:c.6258G>T | XP_011520683.1:p.Thr2086= | |
| XM_005255124.4:c.6966G>T | XP_005255181.1:p.Thr2322= | |
| XM_005255125.4:c.6594G>T | XP_005255182.1:p.Thr2198= | |
| XM_006720848.3:c.6750G>T | XP_006720911.1:p.Thr2250= | |
| XM_011522381.2:c.6258G>T | XP_011520683.1:p.Thr2086= | |
| XM_017022944.1:c.7005G>T | XP_016878433.1:p.Thr2335= | |
| NM_004380.3:c.7011G>T MANE Select | NP_004371.2:p.Thr2337= |