Linked Data
gnomAD v4:
19-7526779-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7526779G>T , CM000681.2:g.7526779G>T | GRCh38 |
| NC_000019.9:g.7591665G>T , CM000681.1:g.7591665G>T | GRCh37 |
| NC_000019.8:g.7497665G>T | NCBI36 |
| NG_015806.1:g.9170G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.424G>T MANE Select | ENSP00000264079.5:p.Val142Leu | |
| ENST00000264079.10:c.424G>T | ENSP00000264079.5:p.Val142Leu | |
| ENST00000394321.9:n.504G>T | ||
| ENST00000596008.1:n.386G>T | ||
| ENST00000598406.1:n.245G>T | ||
| ENST00000601003.1:c.424G>T | ENSP00000469074.1:p.Val142Leu | |
| NM_020533.2:c.424G>T | NP_065394.1:p.Val142Leu | |
| NM_020533.3:c.424G>T MANE Select | NP_065394.1:p.Val142Leu |