Linked Data
gnomAD v4:
20-10412829-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10412829C>T , CM000682.2:g.10412829C>T | GRCh38 |
| NC_000020.10:g.10393477C>T , CM000682.1:g.10393477C>T | GRCh37 |
| NC_000020.9:g.10341477C>T | NCBI36 |
| NG_009109.1:g.26390G>A | |
| NG_009109.2:g.26390G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651692.1:c.686G>A | ENSP00000498849.1:p.Arg229Lys | |
| ENST00000652676.1:n.459-129G>A | ||
| ENST00000347364.7:c.686G>A MANE Select | ENSP00000246062.4:p.Arg229Lys | |
| ENST00000399054.6:c.686G>A | ENSP00000382008.2:p.Arg229Lys | |
| NM_018848.3:c.686G>A | NP_061336.1:p.Arg229Lys | |
| NM_170784.2:c.686G>A | NP_740754.1:p.Arg229Lys | |
| NR_072977.1:n.364-4026G>A | ||
| NR_072977.2:n.347-4026G>A | ||
| NM_170784.3:c.686G>A MANE Select | NP_740754.1:p.Arg229Lys |