Linked Data
gnomAD v4:
12-65246249-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65246249C>T , CM000674.2:g.65246249C>T | GRCh38 |
| NC_000012.11:g.65640029C>T , CM000674.1:g.65640029C>T | GRCh37 |
| NC_000012.10:g.63926296C>T | NCBI36 |
| NG_016210.1:g.81679C>T | |
| NG_016210.2:g.81679C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308330.3:c.2660C>T MANE Select | ENSP00000308369.2:p.Pro887Leu | |
| ENST00000308330.2:c.2660C>T | ENSP00000308369.2:p.Pro887Leu | |
| ENST00000539442.1:n.642C>T | ||
| ENST00000544506.1:n.380C>T | ||
| ENST00000545026.1:n.478C>T | ||
| NM_001167614.1:c.2657C>T | NP_001161086.1:p.Pro886Leu | |
| NM_014319.4:c.2660C>T | NP_055134.2:p.Pro887Leu | |
| NM_014319.5:c.2660C>T MANE Select | NP_055134.2:p.Pro887Leu | |
| NM_001167614.2:c.2657C>T | NP_001161086.1:p.Pro886Leu |