Linked Data
gnomAD v4:
12-14507118-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.14507118C>T , CM000674.2:g.14507118C>T | GRCh38 |
| NC_000012.11:g.14660052C>T , CM000674.1:g.14660052C>T | GRCh37 |
| NC_000012.10:g.14551319C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000240617.10:c.1187G>A MANE Select | ENSP00000240617.5:p.Gly396Glu | |
| ENST00000240617.9:c.1187G>A | ENSP00000240617.5:p.Gly396Glu | |
| NM_024829.5:c.1187G>A | NP_079105.4:p.Gly396Glu | |
| NM_024829.6:c.1187G>A MANE Select | NP_079105.4:p.Gly396Glu |