Linked Data
dbSNP Id:
rs373848722
gnomAD v3:
16-3729596-C-A
gnomAD v4:
16-3729596-C-A
MyVariant Identifiers:
chr16:g.3779597C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3729596C>A , CM000678.2:g.3729596C>A | GRCh38 |
| NC_000016.9:g.3779597C>A , CM000678.1:g.3779597C>A | GRCh37 |
| NC_000016.8:g.3719598C>A | NCBI36 |
| NG_009873.1:g.155525G>T | |
| NG_009873.2:g.156118G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262367.10:c.5451G>T MANE Select | ENSP00000262367.5:p.Pro1817= | |
| ENST00000262367.9:c.5451G>T | ENSP00000262367.5:p.Pro1817= | |
| ENST00000382070.7:c.5337G>T | ENSP00000371502.3:p.Pro1779= | |
| NM_001079846.1:c.5337G>T | NP_001073315.1:p.Pro1779= | |
| NM_004380.2:c.5451G>T | NP_004371.2:p.Pro1817= | |
| XM_005255124.3:c.5406G>T | XP_005255181.1:p.Pro1802= | |
| XM_005255125.3:c.5034G>T | XP_005255182.1:p.Pro1678= | |
| XM_006720848.2:c.5190G>T | XP_006720911.1:p.Pro1730= | |
| XM_011522380.1:c.5397G>T | XP_011520682.1:p.Pro1799= | |
| XM_011522381.1:c.4698G>T | XP_011520683.1:p.Pro1566= | |
| XM_005255124.4:c.5406G>T | XP_005255181.1:p.Pro1802= | |
| XM_005255125.4:c.5034G>T | XP_005255182.1:p.Pro1678= | |
| XM_006720848.3:c.5190G>T | XP_006720911.1:p.Pro1730= | |
| XM_011522381.2:c.4698G>T | XP_011520683.1:p.Pro1566= | |
| XM_017022944.1:c.5445G>T | XP_016878433.1:p.Pro1815= | |
| NM_004380.3:c.5451G>T MANE Select | NP_004371.2:p.Pro1817= |