Linked Data
gnomAD v4:
19-7528055-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7528055G>T , CM000681.2:g.7528055G>T | GRCh38 |
| NC_000019.9:g.7592941G>T , CM000681.1:g.7592941G>T | GRCh37 |
| NC_000019.8:g.7498941G>T | NCBI36 |
| NG_015806.1:g.10446G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.777+95G>T MANE Select | ENSP00000264079.5:n.777+95G>T | |
| ENST00000264079.10:c.777+95G>T | ENSP00000264079.5:n.777+95G>T | |
| ENST00000394321.9:n.1092+95G>T | ||
| NM_020533.2:c.777+95G>T | NP_065394.1:n.777+95G>T | |
| NM_020533.3:c.777+95G>T MANE Select | NP_065394.1:n.777+95G>T |