Linked Data
gnomAD v4:
19-7524815-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7524815T>C , CM000681.2:g.7524815T>C | GRCh38 |
| NC_000019.9:g.7589701T>C , CM000681.1:g.7589701T>C | GRCh37 |
| NC_000019.8:g.7495701T>C | NCBI36 |
| NG_015806.1:g.7206T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.32-146T>C MANE Select | ENSP00000264079.5:n.32-146T>C | |
| ENST00000264079.10:c.32-146T>C | ENSP00000264079.5:n.32-146T>C | |
| ENST00000394321.9:n.112-146T>C | ||
| ENST00000596390.1:n.148-146T>C | ||
| ENST00000601003.1:c.32-146T>C | ENSP00000469074.1:n.32-146T>C | |
| NM_020533.2:c.32-146T>C | NP_065394.1:n.32-146T>C | |
| XR_936293.1:n.140A>G | ||
| XR_936294.1:n.140A>G | ||
| XR_936295.1:n.140A>G | ||
| XR_936293.2:n.166A>G | ||
| XR_936294.2:n.166A>G | ||
| NM_020533.3:c.32-146T>C MANE Select | NP_065394.1:n.32-146T>C |