Linked Data
MyVariant Identifiers:
chr5:g.96350796G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.97015092G>T , CM000667.2:g.97015092G>T | GRCh38 |
| NC_000005.9:g.96350796G>T , CM000667.1:g.96350796G>T | GRCh37 |
| NC_000005.8:g.96376552G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000231368.10:c.2373G>T MANE Select | ENSP00000231368.5:p.Leu791= | |
| ENST00000231368.9:c.2373G>T | ENSP00000231368.5:p.Leu791= | |
| ENST00000395770.3:c.2331G>T | ENSP00000379117.3:p.Leu777= | |
| NM_005575.2:c.2373G>T | NP_005566.2:p.Leu791= | |
| NM_175920.3:c.2331G>T | NP_787116.2:p.Leu777= | |
| XM_024446045.1:c.2373G>T | XP_024301813.1:p.Leu791= | |
| NM_005575.3:c.2373G>T MANE Select | NP_005566.2:p.Leu791= | |
| NM_175920.4:c.2331G>T | NP_787116.2:p.Leu777= |