Linked Data
gnomAD v4:
8-64616129-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.64616129G>T , CM000670.2:g.64616129G>T | GRCh38 |
| NC_000008.10:g.65528686G>T , CM000670.1:g.65528686G>T | GRCh37 |
| NC_000008.9:g.65691240G>T | NCBI36 |
| NG_008338.1:g.187663C>A | |
| NG_008338.2:g.187663C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310193.4:c.412C>A MANE Select | ENSP00000310721.3:p.Leu138Ile | |
| ENST00000310193.3:c.412C>A | ENSP00000310721.3:p.Leu138Ile | |
| NM_004820.3:c.412C>A | NP_004811.1:p.Leu138Ile | |
| NM_001324112.1:c.412C>A | NP_001311041.1:p.Leu138Ile | |
| NM_004820.4:c.412C>A | NP_004811.1:p.Leu138Ile | |
| XM_017014002.1:c.478C>A | XP_016869491.1:p.Leu160Ile | |
| NM_004820.5:c.412C>A MANE Select | NP_004811.1:p.Leu138Ile | |
| NM_001324112.2:c.412C>A | NP_001311041.1:p.Leu138Ile |