Linked Data
gnomAD v4:
6-112069770-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.112069770G>T , CM000668.2:g.112069770G>T | GRCh38 |
| NC_000006.11:g.112390973G>T , CM000668.1:g.112390973G>T | GRCh37 |
| NC_000006.10:g.112497666G>T | NCBI36 |
| NG_011748.1:g.20696G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361714.5:c.*150G>T | ENSP00000354734.2:n.*150G>T | |
| ENST00000368666.6:c.*150G>T | ENSP00000357655.3:n.*150G>T |