Linked Data
dbSNP Id:
rs752159331
ExAC:
16:88901642 G / C
gnomAD v2:
16-88901642-G-C
gnomAD v4:
16-88835234-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88835234G>C , CM000678.2:g.88835234G>C | GRCh38 |
| NC_000016.9:g.88901642G>C , CM000678.1:g.88901642G>C | GRCh37 |
| NC_000016.8:g.87429143G>C | NCBI36 |
| NG_008667.1:g.26733C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268695.10:c.877C>G MANE Select | ENSP00000268695.5:p.Leu293Val | |
| ENST00000268695.9:c.877C>G | ENSP00000268695.5:p.Leu293Val | |
| ENST00000562593.5:n.4286C>G | ||
| ENST00000562931.5:n.465C>G | ||
| ENST00000567525.5:c.558C>G | ENSP00000454484.1:n.558C>G | |
| ENST00000568613.5:c.996C>G | ENSP00000457921.1:n.996C>G | |
| NM_000512.4:c.877C>G | NP_000503.1:p.Leu293Val | |
| XM_005256301.2:c.877C>G | XP_005256358.1:p.Leu293Val | |
| XM_005256302.1:c.895C>G | XP_005256359.1:p.Leu299Val | |
| XM_011522982.1:c.895C>G | XP_011521284.1:p.Leu299Val | |
| XM_011522984.1:c.895C>G | XP_011521286.1:p.Leu299Val | |
| NM_001323543.1:c.322C>G | NP_001310472.1:p.Leu108Val | |
| NM_001323544.1:c.895C>G | NP_001310473.1:p.Leu299Val | |
| XM_005256301.3:c.877C>G | XP_005256358.1:p.Leu293Val | |
| XM_011522982.2:c.895C>G | XP_011521284.1:p.Leu299Val | |
| XM_017023111.2:c.895C>G | XP_016878600.1:p.Leu299Val | |
| XM_017023112.2:c.895C>G | XP_016878601.1:p.Leu299Val | |
| XM_017023113.1:c.322C>G | XP_016878602.1:p.Leu108Val | |
| NM_000512.5:c.877C>G MANE Select | NP_000503.1:p.Leu293Val | |
| NM_001323543.2:c.322C>G | NP_001310472.1:p.Leu108Val | |
| NM_001323544.2:c.895C>G | NP_001310473.1:p.Leu299Val |