Linked Data
gnomAD v4:
2-47783014-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47783014G>T , CM000664.2:g.47783014G>T | GRCh38 |
| NC_000002.11:g.48010153G>T , CM000664.1:g.48010153G>T | GRCh37 |
| NC_000002.10:g.47863657G>T | NCBI36 |
| NG_007111.1:g.4868G>T , LRG_219:g.4868G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000652107.1:c.-37-7913G>T | ENSP00000498629.1:n.-37-7913G>T | |
| ENST00000606499.1:c.-37-7913G>T | ENSP00000475605.1:n.-37-7913G>T |