Linked Data
MyVariant Identifiers:
chr1:g.68895555G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68429872G>T , CM000663.2:g.68429872G>T | GRCh38 |
| NC_000001.10:g.68895555G>T , CM000663.1:g.68895555G>T | GRCh37 |
| NC_000001.9:g.68668143G>T | NCBI36 |
| NG_008472.1:g.25088C>A | |
| NG_008472.2:g.25088C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1506C>A MANE Select | ENSP00000262340.5:p.Leu502= | |
| ENST00000262340.5:c.1506C>A | ENSP00000262340.5:p.Leu502= | |
| NM_000329.2:c.1506C>A | NP_000320.1:p.Leu502= | |
| XM_017002027.1:c.1230C>A | XP_016857516.1:p.Leu410= | |
| NM_000329.3:c.1506C>A MANE Select | NP_000320.1:p.Leu502= |