Linked Data
MyVariant Identifiers:
chr1:g.213056765A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.212883423A>C , CM000663.2:g.212883423A>C | GRCh38 |
| NC_000001.10:g.213056765A>C , CM000663.1:g.213056765A>C | GRCh37 |
| NC_000001.9:g.211123388A>C | NCBI36 |
| NG_028131.1:g.30169A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366971.9:c.1077A>C MANE Select | ENSP00000355938.4:p.Ile359= | |
| ENST00000366971.8:c.1077A>C | ENSP00000355938.4:p.Ile359= | |
| ENST00000419102.1:c.473A>C | ||
| ENST00000474693.1:n.302A>C | ||
| ENST00000483790.1:n.15A>C | ||
| NM_014053.3:c.1077A>C | NP_054772.1:p.Ile359= | |
| XM_011509446.1:c.1077A>C | XP_011507748.1:p.Ile359= | |
| XR_247024.1:n.1251A>C | ||
| XR_426771.1:n.1378A>C | ||
| XM_011509446.3:c.1077A>C | XP_011507748.1:p.Ile359= | |
| XR_247024.3:n.1251A>C | ||
| NM_014053.4:c.1077A>C MANE Select | NP_054772.1:p.Ile359= |