Linked Data
gnomAD v4:
16-67942972-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67942972C>T , CM000678.2:g.67942972C>T | GRCh38 |
| NC_000016.9:g.67976875C>T , CM000678.1:g.67976875C>T | GRCh37 |
| NC_000016.8:g.66534376C>T | NCBI36 |
| NG_009778.1:g.6141G>A | |
| NG_033098.1:g.30723G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264005.10:c.316G>A MANE Select | ENSP00000264005.5:p.Val106Ile | |
| ENST00000264005.9:c.316G>A | ENSP00000264005.5:p.Val106Ile | |
| ENST00000570369.5:c.44G>A | ||
| ENST00000570980.1:c.100G>A | ENSP00000464651.1:p.Val34Ile | |
| ENST00000575277.1:n.94G>A | ||
| ENST00000575467.5:c.*11G>A | ENSP00000460653.1:n.*11G>A | |
| NM_000229.1:c.316G>A | NP_000220.1:p.Val106Ile | |
| NM_000229.2:c.316G>A MANE Select | NP_000220.1:p.Val106Ile |