Linked Data
gnomAD v4:
6-44313411-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.44313411G>T , CM000668.2:g.44313411G>T | GRCh38 |
| NC_000006.11:g.44281148G>T , CM000668.1:g.44281148G>T | GRCh37 |
| NC_000006.10:g.44389126G>T | NCBI36 |
| NG_031952.1:g.4916C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000505802.1:c.855+5769G>T | ||
| NM_001318876.2:c.946-128479G>T | NP_001305805.1:n.946-128479G>T |