Linked Data
dbSNP Id:
rs1307256288
gnomAD v2:
16-16110469-C-G
gnomAD v3:
16-16016612-C-G
gnomAD v4:
16-16016612-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16016612C>G , CM000678.2:g.16016612C>G | GRCh38 |
| NC_000016.9:g.16110469C>G , CM000678.1:g.16110469C>G | GRCh37 |
| NC_000016.8:g.16017970C>G | NCBI36 |
| NG_028268.1:g.72036C>G | |
| NG_028268.2:g.72036C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399408.7:c.606C>G | ENSP00000382340.4:p.Ile202Met | |
| ENST00000399410.8:c.606C>G MANE Select | ENSP00000382342.3:p.Ile202Met | |
| ENST00000572882.3:c.606C>G | ENSP00000461615.2:p.Ile202Met | |
| ENST00000574224.2:n.681C>G | ||
| ENST00000677164.1:c.489+1984C>G | ENSP00000502873.1:n.489+1984C>G | |
| ENST00000678422.1:c.606C>G | ENSP00000503954.1:p.Ile202Met | |
| ENST00000679043.1:n.558C>G | ||
| ENST00000399408.6:c.-373C>G | ENSP00000382340.3:n.-373C>G | |
| ENST00000399410.7:c.606C>G | ENSP00000382342.3:p.Ile202Met | |
| ENST00000572882.2:c.301C>G | ||
| ENST00000574224.1:n.206C>G | ||
| NM_004996.3:c.606C>G | NP_004987.2:p.Ile202Met | |
| XM_011522497.1:c.582C>G | XP_011520799.1:p.Ile194Met | |
| XM_011522498.1:c.660C>G | XP_011520800.1:p.Ile220Met | |
| XM_011522498.2:c.660C>G | XP_011520800.1:p.Ile220Met | |
| XM_017023237.1:c.660C>G | XP_016878726.1:p.Ile220Met | |
| XM_017023238.1:c.543+1984C>G | XP_016878727.1:n.543+1984C>G | |
| XM_017023239.1:c.522C>G | XP_016878728.1:p.Ile174Met | |
| XM_017023240.1:c.660C>G | XP_016878729.1:p.Ile220Met | |
| XM_017023241.1:c.405+6711C>G | XP_016878730.1:n.405+6711C>G | |
| XM_017023242.1:c.660C>G | XP_016878731.1:p.Ile220Met | |
| XM_017023243.2:c.660C>G | XP_016878732.1:p.Ile220Met | |
| NM_004996.4:c.606C>G MANE Select | NP_004987.2:p.Ile202Met |