Linked Data
ClinVar Variation Id:
2082136
ClinVar RCV Id:
RCV002995834
MyVariant Identifiers:
chr16:g.3900340A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3850339A>G , CM000678.2:g.3850339A>G | GRCh38 |
| NC_000016.9:g.3900340A>G , CM000678.1:g.3900340A>G | GRCh37 |
| NC_000016.8:g.3840341A>G | NCBI36 |
| NG_009873.1:g.34782T>C | |
| NG_009873.2:g.35375T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262367.10:c.756T>C MANE Select | ENSP00000262367.5:p.Gly252= | |
| ENST00000262367.9:c.756T>C | ENSP00000262367.5:p.Gly252= | |
| ENST00000382070.7:c.756T>C | ENSP00000371502.3:p.Gly252= | |
| NM_001079846.1:c.756T>C | NP_001073315.1:p.Gly252= | |
| NM_004380.2:c.756T>C | NP_004371.2:p.Gly252= | |
| XM_005255124.3:c.756T>C | XP_005255181.1:p.Gly252= | |
| XM_005255125.3:c.756T>C | XP_005255182.1:p.Gly252= | |
| XM_006720848.2:c.756T>C | XP_006720911.1:p.Gly252= | |
| XM_011522380.1:c.702T>C | XP_011520682.1:p.Gly234= | |
| XM_011522382.1:c.756T>C | XP_011520684.1:p.Gly252= | |
| XM_005255124.4:c.756T>C | XP_005255181.1:p.Gly252= | |
| XM_005255125.4:c.756T>C | XP_005255182.1:p.Gly252= | |
| XM_006720848.3:c.756T>C | XP_006720911.1:p.Gly252= | |
| XM_011522382.3:c.756T>C | XP_011520684.1:p.Gly252= | |
| XM_017022944.1:c.756T>C | XP_016878433.1:p.Gly252= | |
| NM_004380.3:c.756T>C MANE Select | NP_004371.2:p.Gly252= |