Linked Data
dbSNP Id:
rs767895645
ExAC:
15:89872306 C / T
gnomAD v2:
15-89872306-C-T
gnomAD v4:
15-89329075-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89329075C>T , CM000677.2:g.89329075C>T | GRCh38 |
| NC_000015.9:g.89872306C>T , CM000677.1:g.89872306C>T | GRCh37 |
| NC_000015.8:g.87673310C>T | NCBI36 |
| NG_008218.1:g.10721G>A | |
| NG_008218.2:g.10721G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636937.2:c.891G>A | ENSP00000516154.1:p.Met297Ile | |
| ENST00000268124.11:c.891G>A MANE Select | ENSP00000268124.5:p.Met297Ile | |
| ENST00000530292.3:c.492G>A | ENSP00000432885.2:p.Met164Ile | |
| ENST00000635986.2:c.891G>A | ENSP00000490653.2:p.Met297Ile | |
| ENST00000636774.1:c.891G>A | ENSP00000489799.1:p.Met297Ile | |
| ENST00000666746.1:c.548G>A | ||
| ENST00000672071.1:n.1089G>A | ||
| ENST00000268124.9:c.891G>A | ENSP00000268124.5:p.Met297Ile | |
| ENST00000442287.6:c.891G>A | ENSP00000399851.2:p.Met297Ile | |
| ENST00000631044.2:c.*274G>A | ENSP00000486730.1:n.*274G>A | |
| NM_001126131.1:c.891G>A | NP_001119603.1:p.Met297Ile | |
| NM_002693.2:c.891G>A | NP_002684.1:p.Met297Ile | |
| NM_001126131.2:c.891G>A | NP_001119603.1:p.Met297Ile | |
| NM_002693.3:c.891G>A MANE Select | NP_002684.1:p.Met297Ile |