Linked Data
gnomAD v4:
12-10445972-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.10445972A>T , CM000674.2:g.10445972A>T | GRCh38 |
| NC_000012.11:g.10598571A>T , CM000674.1:g.10598571A>T | GRCh37 |
| NC_000012.10:g.10489838A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000536188.5:c.685+596T>A | ENSP00000441432.1:n.685+596T>A | |
| NM_001304448.1:c.685+596T>A | NP_001291377.1:n.685+596T>A | |
| XM_024448973.1:c.685+596T>A | XP_024304741.1:n.685+596T>A |