Linked Data
gnomAD v4:
6-44313363-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.44313363C>T , CM000668.2:g.44313363C>T | GRCh38 |
| NC_000006.11:g.44281100C>T , CM000668.1:g.44281100C>T | GRCh37 |
| NC_000006.10:g.44389078C>T | NCBI36 |
| NG_031952.1:g.4964G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000505802.1:c.855+5721C>T | ||
| NM_001318876.2:c.946-128527C>T | NP_001305805.1:n.946-128527C>T |