Linked Data
gnomAD v4:
2-47783029-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47783029C>T , CM000664.2:g.47783029C>T | GRCh38 |
| NC_000002.11:g.48010168C>T , CM000664.1:g.48010168C>T | GRCh37 |
| NC_000002.10:g.47863672C>T | NCBI36 |
| NG_007111.1:g.4883C>T , LRG_219:g.4883C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000652107.1:c.-37-7898C>T | ENSP00000498629.1:n.-37-7898C>T | |
| ENST00000606499.1:c.-37-7898C>T | ENSP00000475605.1:n.-37-7898C>T |