Linked Data
gnomAD v4:
19-39243573-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.39243573A>G , CM000681.2:g.39243573A>G | GRCh38 |
| NC_000019.9:g.39734213A>G , CM000681.1:g.39734213A>G | GRCh37 |
| NC_000019.8:g.44426053A>G | NCBI36 |
| NG_042193.1:g.6399T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613087.5:c.*59T>C | ENSP00000481633.1:n.*59T>C | |
| ENST00000413851.3:c.*59T>C MANE Select | ENSP00000409000.2:n.*59T>C | |
| ENST00000613087.4:c.*59T>C | ENSP00000481633.1:n.*59T>C | |
| NM_172139.4:c.*59T>C MANE Select | NP_742151.2:n.*59T>C | |
| NM_001346937.2:c.*59T>C | NP_001333866.1:n.*59T>C |