Linked Data
gnomAD v4:
11-64753556-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64753556C>A , CM000673.2:g.64753556C>A | GRCh38 |
| NC_000011.9:g.64521028C>A , CM000673.1:g.64521028C>A | GRCh37 |
| NC_000011.8:g.64277604C>A | NCBI36 |
| NG_013018.1:g.12160G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000164139.4:c.1366G>T MANE Select | ENSP00000164139.3:p.Val456Leu | |
| ENST00000164139.3:c.1366G>T | ENSP00000164139.3:p.Val456Leu | |
| ENST00000377432.7:c.1102G>T | ENSP00000366650.3:p.Val368Leu | |
| NM_001164716.1:c.1102G>T | NP_001158188.1:p.Val368Leu | |
| NM_005609.2:c.1366G>T | NP_005600.1:p.Val456Leu | |
| NM_005609.3:c.1366G>T | NP_005600.1:p.Val456Leu | |
| NM_005609.4:c.1366G>T MANE Select | NP_005600.1:p.Val456Leu |