Linked Data
MyVariant Identifiers:
chr12:g.103234173_103234179del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102840395_102840401del , CM000674.2:g.102840395_102840401del | GRCh38 |
| NC_000012.11:g.103234173_103234179del , CM000674.1:g.103234173_103234179del | GRCh37 |
| NC_000012.10:g.101758303_101758309del | NCBI36 |
| NG_008690.1:g.82202_82208del | |
| NG_008690.2:g.123010_123016del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553106.6:c.1314_1315+5del | ||
| ENST00000307000.7:c.1299_1300+5del | ||
| ENST00000551114.2:n.976_977+5del | ||
| ENST00000553106.5:c.1314_1315+5del | ||
| ENST00000635477.1:c.418_419+5del | ||
| ENST00000635528.1:n.829_830+5del | ||
| NM_000277.1:c.1314_1315+5del | ||
| XM_011538422.1:c.1257_1258+5del | ||
| NM_000277.2:c.1314_1315+5del | ||
| NM_001354304.1:c.1314_1315+5del | ||
| NM_000277.3:c.1314_1315+5del | ||
| NM_001354304.2:c.1314_1315+5del |