Linked Data
gnomAD v4:
12-10445963-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.10445963A>G , CM000674.2:g.10445963A>G | GRCh38 |
| NC_000012.11:g.10598562A>G , CM000674.1:g.10598562A>G | GRCh37 |
| NC_000012.10:g.10489829A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000536188.5:c.685+605T>C | ENSP00000441432.1:n.685+605T>C | |
| NM_001304448.1:c.685+605T>C | NP_001291377.1:n.685+605T>C | |
| XM_024448973.1:c.685+605T>C | XP_024304741.1:n.685+605T>C |