Linked Data
dbSNP Id:
rs764544505
ExAC:
10:124266215 G / C
gnomAD v2:
10-124266215-G-C
gnomAD v4:
10-122506699-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122506699G>C , CM000672.2:g.122506699G>C | GRCh38 |
| NC_000010.10:g.124266215G>C , CM000672.1:g.124266215G>C | GRCh37 |
| NC_000010.9:g.124256205G>C | NCBI36 |
| NG_011554.1:g.50175G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.786G>C MANE Select | ENSP00000357980.3:p.Leu262= | |
| ENST00000648167.1:c.468G>C | ENSP00000498033.1:p.Leu156= | |
| ENST00000368984.7:c.786G>C | ENSP00000357980.3:p.Leu262= | |
| ENST00000420892.1:c.9G>C | ENSP00000412676.1:p.Leu3= | |
| NM_002775.4:c.786G>C | NP_002766.1:p.Leu262= | |
| NM_002775.5:c.786G>C MANE Select | NP_002766.1:p.Leu262= |