Linked Data
gnomAD v4:
12-65246296-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65246296G>A , CM000674.2:g.65246296G>A | GRCh38 |
| NC_000012.11:g.65640076G>A , CM000674.1:g.65640076G>A | GRCh37 |
| NC_000012.10:g.63926343G>A | NCBI36 |
| NG_016210.1:g.81726G>A | |
| NG_016210.2:g.81726G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.2707G>A MANE Select | ENSP00000308369.2:p.Gly903Ser | |
| ENST00000308330.2:c.2707G>A | ENSP00000308369.2:p.Gly903Ser | |
| ENST00000539442.1:n.689G>A | ||
| ENST00000545026.1:n.525G>A | ||
| NM_001167614.1:c.2704G>A | NP_001161086.1:p.Gly902Ser | |
| NM_014319.4:c.2707G>A | NP_055134.2:p.Gly903Ser | |
| NM_014319.5:c.2707G>A MANE Select | NP_055134.2:p.Gly903Ser | |
| NM_001167614.2:c.2704G>A | NP_001161086.1:p.Gly902Ser |