MyVariant.info:
GRCh37
chr16:g.3790455G>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3740454G>T , CM000678.2:g.3740454G>T | GRCh38 |
| NC_000016.9:g.3790455G>T , CM000678.1:g.3790455G>T | GRCh37 |
| NC_000016.8:g.3730456G>T | NCBI36 |
| NG_009873.1:g.144667C>A | |
| NG_009873.2:g.145260C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262367.10:c.4078C>A MANE Select | ENSP00000262367.5:p.Arg1360= | |
| ENST00000262367.9:c.4078C>A | ENSP00000262367.5:p.Arg1360= | |
| ENST00000382070.7:c.3964C>A | ENSP00000371502.3:p.Arg1322= | |
| ENST00000570939.2:c.2713C>A | ENSP00000461002.2:p.Arg905= | |
| ENST00000572569.1:n.542C>A | ||
| ENST00000573517.6:c.384C>A | ||
| ENST00000574740.1:n.160C>A | ||
| ENST00000576720.1:n.3015C>A | ||
| NM_001079846.1:c.3964C>A | NP_001073315.1:p.Arg1322= | |
| NM_004380.2:c.4078C>A | NP_004371.2:p.Arg1360= | |
| XM_005255124.3:c.4033C>A | XP_005255181.1:p.Arg1345= | |
| XM_005255125.3:c.3661C>A | XP_005255182.1:p.Arg1221= | |
| XM_006720848.2:c.4078C>A | XP_006720911.1:p.Arg1360= | |
| XM_011522380.1:c.4024C>A | XP_011520682.1:p.Arg1342= | |
| XM_011522381.1:c.3325C>A | XP_011520683.1:p.Arg1109= | |
| XM_005255124.4:c.4033C>A | XP_005255181.1:p.Arg1345= | |
| XM_005255125.4:c.3661C>A | XP_005255182.1:p.Arg1221= | |
| XM_006720848.3:c.4078C>A | XP_006720911.1:p.Arg1360= | |
| XM_011522381.2:c.3325C>A | XP_011520683.1:p.Arg1109= | |
| XM_017022944.1:c.4072C>A | XP_016878433.1:p.Arg1358= | |
| NM_004380.3:c.4078C>A MANE Select | NP_004371.2:p.Arg1360= |