Linked Data
gnomAD v4:
14-102922696-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.102922696T>C , CM000676.2:g.102922696T>C | GRCh38 |
| NC_000014.8:g.103389033T>C , CM000676.1:g.103389033T>C | GRCh37 |
| NC_000014.7:g.102458786T>C | NCBI36 |
| NG_008276.2:g.5041T>C , LRG_642:g.5041T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299155.10:c.8T>C MANE Select | ENSP00000299155.6:p.Val3Ala | |
| ENST00000299155.9:c.8T>C | ENSP00000299155.5:p.Val3Ala | |
| NM_030943.3:c.8T>C , LRG_642t1:c.8T>C | NP_112205.2:p.Val3Ala | |
| XM_011537202.1:c.-174T>C | XP_011535504.1:n.-174T>C | |
| XM_011537202.3:c.-174T>C | XP_011535504.1:n.-174T>C | |
| XM_024449714.1:c.104T>C | XP_024305482.1:p.Val35Ala | |
| NM_030943.4:c.8T>C MANE Select | NP_112205.2:p.Val3Ala |