Linked Data
gnomAD v4:
5-151100780-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.151100780C>T , CM000667.2:g.151100780C>T | GRCh38 |
| NC_000005.9:g.150480341C>T , CM000667.1:g.150480341C>T | GRCh37 |
| NC_000005.8:g.150460534C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354546.10:c.*668G>A MANE Select | ENSP00000346550.5:n.*668G>A | |
| ENST00000522664.5:c.383G>A | ||
| NM_001155.4:c.*668G>A | NP_001146.2:n.*668G>A | |
| NM_001193544.1:c.*668G>A | NP_001180473.1:n.*668G>A | |
| NM_001363114.1:c.*668G>A | NP_001350043.1:n.*668G>A | |
| NM_001155.5:c.*668G>A MANE Select | NP_001146.2:n.*668G>A | |
| NM_001193544.2:c.*668G>A | NP_001180473.1:n.*668G>A | |
| NM_001363114.2:c.*668G>A | NP_001350043.1:n.*668G>A |