Linked Data
ClinVar Variation Id:
2125308
ClinVar RCV Id:
RCV003049511
MyVariant Identifiers:
chr18:g.21136252A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.23556288A>C , CM000680.2:g.23556288A>C | GRCh38 |
| NC_000018.9:g.21136252A>C , CM000680.1:g.21136252A>C | GRCh37 |
| NC_000018.8:g.19390250A>C | NCBI36 |
| NG_012795.1:g.35330T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269228.10:c.1281T>G MANE Select | ENSP00000269228.4:p.Ala427= | |
| ENST00000269228.9:c.1281T>G | ENSP00000269228.4:p.Ala427= | |
| ENST00000540608.5:n.1195T>G | ||
| ENST00000591051.1:c.563T>G | ||
| NM_000271.4:c.1281T>G | NP_000262.2:p.Ala427= | |
| XM_005258277.1:c.1332T>G | XP_005258334.1:p.Ala444= | |
| XM_005258278.3:c.1332T>G | XP_005258335.1:p.Ala444= | |
| XM_005258279.1:c.1281T>G | XP_005258336.1:p.Ala427= | |
| XM_006722479.2:c.1332T>G | XP_006722542.1:p.Ala444= | |
| XM_011526015.1:c.867T>G | XP_011524317.1:p.Ala289= | |
| XM_005258278.5:c.1332T>G | XP_005258335.1:p.Ala444= | |
| XM_005258279.2:c.1281T>G | XP_005258336.1:p.Ala427= | |
| XM_006722479.3:c.1332T>G | XP_006722542.1:p.Ala444= | |
| XM_017025784.1:c.1332T>G | XP_016881273.1:p.Ala444= | |
| XM_017025785.1:c.1332T>G | XP_016881274.1:p.Ala444= | |
| XM_017025786.1:c.1281T>G | XP_016881275.1:p.Ala427= | |
| XM_017025787.1:c.1281T>G | XP_016881276.1:p.Ala427= | |
| NM_000271.5:c.1281T>G MANE Select | NP_000262.2:p.Ala427= |