Linked Data
gnomAD v4:
12-10446017-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.10446017C>A , CM000674.2:g.10446017C>A | GRCh38 |
| NC_000012.11:g.10598616C>A , CM000674.1:g.10598616C>A | GRCh37 |
| NC_000012.10:g.10489883C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000536188.5:c.685+551G>T | ENSP00000441432.1:n.685+551G>T | |
| NM_001304448.1:c.685+551G>T | NP_001291377.1:n.685+551G>T | |
| XM_024448973.1:c.685+551G>T | XP_024304741.1:n.685+551G>T |