Linked Data
gnomAD v4:
1-154571697-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571697C>A , CM000663.2:g.154571697C>A | GRCh38 |
| NC_000001.10:g.154544173C>A , CM000663.1:g.154544173C>A | GRCh37 |
| NC_000001.9:g.152810797C>A | NCBI36 |
| NG_008027.1:g.8917C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.874C>A MANE Select | ENSP00000357461.3:p.Leu292Ile | |
| ENST00000636034.1:c.874C>A | ENSP00000489703.1:p.Leu292Ile | |
| ENST00000637900.1:c.880C>A | ENSP00000490474.1:p.Leu294Ile | |
| ENST00000368476.3:c.874C>A | ENSP00000357461.3:p.Leu292Ile | |
| NM_000748.2:c.874C>A | NP_000739.1:p.Leu292Ile | |
| XM_017000180.2:c.364C>A | XP_016855669.1:p.Leu122Ile | |
| XR_001736952.2:n.1126C>A | ||
| NM_000748.3:c.874C>A MANE Select | NP_000739.1:p.Leu292Ile |