Linked Data
gnomAD v4:
19-47003987-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.47003987C>T , CM000681.2:g.47003987C>T | GRCh38 |
| NC_000019.9:g.47507244C>T , CM000681.1:g.47507244C>T | GRCh37 |
| NC_000019.8:g.52199084C>T | NCBI36 |
| NG_047014.1:g.90421C>T | |
| NG_047014.2:g.147991C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000404338.8:c.7799C>T | ENSP00000385720.2:n.7799C>T | |
| ENST00000672722.1:c.*3299C>T MANE Select | ENSP00000500409.1:n.*3299C>T | |
| ENST00000404338.7:c.7799C>T | ENSP00000385720.2:n.7799C>T | |
| ENST00000614079.1:c.7376C>T | ENSP00000483730.1:n.7376C>T | |
| NM_004491.4:c.7799C>T | NP_004482.4:n.7799C>T | |
| NM_004491.5:c.*3299C>T MANE Select | NP_004482.4:n.*3299C>T |