Linked Data
gnomAD v4:
8-19951842-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19951842T>C , CM000670.2:g.19951842T>C | GRCh38 |
| NC_000008.10:g.19809353T>C , CM000670.1:g.19809353T>C | GRCh37 |
| NC_000008.9:g.19853633T>C | NCBI36 |
| NG_008855.1:g.17772T>C | |
| NG_008855.2:g.55126T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.323T>C MANE Select | ENSP00000497642.1:p.Val108Ala | |
| ENST00000311322.8:c.323T>C | ENSP00000309757.6:p.Val108Ala | |
| ENST00000520959.5:c.95T>C | ENSP00000428496.1:p.Val32Ala | |
| ENST00000524029.5:c.323T>C | ENSP00000428237.1:p.Val108Ala | |
| NM_000237.2:c.323T>C | NP_000228.1:p.Val108Ala | |
| NM_000237.3:c.323T>C MANE Select | NP_000228.1:p.Val108Ala |