Linked Data
gnomAD v4:
11-64747439-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64747439C>A , CM000673.2:g.64747439C>A | GRCh38 |
| NC_000011.9:g.64514911C>A , CM000673.1:g.64514911C>A | GRCh37 |
| NC_000011.8:g.64271487C>A | NCBI36 |
| NG_007574.1:g.3018G>T , LRG_100:g.3018G>T | |
| NG_013018.1:g.18277G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000164139.4:c.2178-81G>T MANE Select | ENSP00000164139.3:n.2178-81G>T | |
| ENST00000164139.3:c.2178-81G>T | ENSP00000164139.3:n.2178-81G>T | |
| ENST00000377432.7:c.1914-81G>T | ENSP00000366650.3:n.1914-81G>T | |
| ENST00000483742.1:n.1450G>T | ||
| NM_001164716.1:c.1914-81G>T | NP_001158188.1:n.1914-81G>T | |
| NM_005609.2:c.2178-81G>T | NP_005600.1:n.2178-81G>T | |
| NM_005609.3:c.2178-81G>T | NP_005600.1:n.2178-81G>T | |
| NM_005609.4:c.2178-81G>T MANE Select | NP_005600.1:n.2178-81G>T |