Linked Data
gnomAD v4:
2-47783002-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47783002A>C , CM000664.2:g.47783002A>C | GRCh38 |
| NC_000002.11:g.48010141A>C , CM000664.1:g.48010141A>C | GRCh37 |
| NC_000002.10:g.47863645A>C | NCBI36 |
| NG_007111.1:g.4856A>C , LRG_219:g.4856A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000652107.1:c.-37-7925A>C | ENSP00000498629.1:n.-37-7925A>C | |
| ENST00000606499.1:c.-37-7925A>C | ENSP00000475605.1:n.-37-7925A>C |