Linked Data
gnomAD v4:
3-147413463-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.147413463C>T , CM000665.2:g.147413463C>T | GRCh38 |
| NC_000003.11:g.147131250C>T , CM000665.1:g.147131250C>T | GRCh37 |
| NC_000003.10:g.148613940C>T | NCBI36 |
| NG_015886.1:g.9070C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000282928.5:c.1256C>T MANE Select | ENSP00000282928.4:p.Thr419Ile | |
| ENST00000282928.4:c.1256C>T | ENSP00000282928.4:p.Thr419Ile | |
| ENST00000472523.1:n.521+19521C>T | ||
| ENST00000488404.5:c.322C>T | ||
| NM_003412.3:c.1256C>T | NP_003403.2:p.Thr419Ile | |
| NM_003412.4:c.1256C>T MANE Select | NP_003403.2:p.Thr419Ile |