Linked Data
gnomAD v4:
X-29399302-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.29399302G>A , CM000685.2:g.29399302G>A | GRCh38 |
| NC_000023.10:g.29417419G>A , CM000685.1:g.29417419G>A | GRCh37 |
| NC_000023.9:g.29327340G>A | NCBI36 |
| NG_008292.1:g.816739G>A | |
| NG_008292.2:g.816739G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378993.6:c.697G>A MANE Select | ENSP00000368278.1:p.Val233Ile | |
| ENST00000378993.5:c.697G>A | ENSP00000368278.1:p.Val233Ile | |
| NM_014271.3:c.697G>A | NP_055086.1:p.Val233Ile | |
| XM_005274441.1:c.697G>A | XP_005274498.1:p.Val233Ile | |
| XM_011545445.1:c.697G>A | XP_011543747.1:p.Val233Ile | |
| XM_017029240.1:c.697G>A | XP_016884729.1:p.Val233Ile | |
| XM_017029241.1:c.319G>A | XP_016884730.1:p.Val107Ile | |
| NM_014271.4:c.697G>A MANE Select | NP_055086.1:p.Val233Ile |