Linked Data
gnomAD v4:
6-135497787-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.135497787A>C , CM000668.2:g.135497787A>C | GRCh38 |
| NC_000006.11:g.135818925A>C , CM000668.1:g.135818925A>C | GRCh37 |
| NC_000006.10:g.135860618A>C | NCBI36 |
| NG_008643.1:g.4979T>G | |
| NG_008643.2:g.4979T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680033.1:c.-2303T>G | ENSP00000506426.1:n.-2303T>G | |
| ENST00000681022.1:c.-2303T>G | ENSP00000505121.1:n.-2303T>G |