Linked Data
gnomAD v4:
5-128357366-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128357366C>T , CM000667.2:g.128357366C>T | GRCh38 |
| NC_000005.9:g.127693058C>T , CM000667.1:g.127693058C>T | GRCh37 |
| NC_000005.8:g.127720957C>T | NCBI36 |
| NG_008750.1:g.185678G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262464.9:c.2584G>A MANE Select | ENSP00000262464.4:p.Val862Ile | |
| ENST00000262464.8:c.2584G>A | ENSP00000262464.4:p.Val862Ile | |
| ENST00000508053.5:c.2584G>A | ENSP00000424571.1:p.Val862Ile | |
| ENST00000508989.5:c.2485G>A | ENSP00000425596.1:p.Val829Ile | |
| ENST00000619499.4:c.2581G>A | ENSP00000482132.1:p.Val861Ile | |
| NM_001999.3:c.2584G>A | NP_001990.2:p.Val862Ile | |
| XM_017009228.2:c.2431G>A | XP_016864717.1:p.Val811Ile | |
| NM_001999.4:c.2584G>A MANE Select | NP_001990.2:p.Val862Ile |