Linked Data
gnomAD v4:
19-47004275-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.47004275T>C , CM000681.2:g.47004275T>C | GRCh38 |
| NC_000019.9:g.47507532T>C , CM000681.1:g.47507532T>C | GRCh37 |
| NC_000019.8:g.52199372T>C | NCBI36 |
| NG_047014.1:g.90709T>C | |
| NG_047014.2:g.148279T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000404338.8:c.8087T>C | ENSP00000385720.2:n.8087T>C | |
| ENST00000672722.1:c.*3587T>C MANE Select | ENSP00000500409.1:n.*3587T>C | |
| ENST00000404338.7:c.8087T>C | ENSP00000385720.2:n.8087T>C | |
| ENST00000614079.1:c.7664T>C | ENSP00000483730.1:n.7664T>C | |
| NM_004491.4:c.8087T>C | NP_004482.4:n.8087T>C | |
| NM_004491.5:c.*3587T>C MANE Select | NP_004482.4:n.*3587T>C |