Linked Data
gnomAD v4:
19-7533972-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7533972G>T , CM000681.2:g.7533972G>T | GRCh38 |
| NC_000019.9:g.7598858G>T , CM000681.1:g.7598858G>T | GRCh37 |
| NC_000019.8:g.7504858G>T | NCBI36 |
| NG_013374.1:g.4821G>T | |
| NG_015806.1:g.16363G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.*177G>T MANE Select | ENSP00000264079.5:n.*177G>T | |
| ENST00000264079.10:c.*177G>T | ENSP00000264079.5:n.*177G>T | |
| ENST00000394321.9:n.2235G>T | ||
| ENST00000599334.1:c.648G>T | ||
| ENST00000601870.1:c.169+104G>T | ||
| ENST00000602227.1:n.474G>T | ||
| NM_020533.2:c.*177G>T | NP_065394.1:n.*177G>T | |
| NM_020533.3:c.*177G>T MANE Select | NP_065394.1:n.*177G>T |