Linked Data
gnomAD v4:
6-1609969-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1609969G>T , CM000668.2:g.1609969G>T | GRCh38 |
| NC_000006.11:g.1610204G>T , CM000668.1:g.1610204G>T | GRCh37 |
| NC_000006.10:g.1555203G>T | NCBI36 |
| NG_009368.1:g.4524G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.-477G>T MANE Select | ENSP00000493906.1:n.-477G>T | |
| NM_001453.3:c.-477G>T MANE Select | NP_001444.2:n.-477G>T |