Linked Data
dbSNP Id:
rs755293105
gnomAD v3:
11-67585226-C-G
gnomAD v4:
11-67585226-C-G
MyVariant Identifiers:
chr11:g.67352697C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67585226C>G , CM000673.2:g.67585226C>G | GRCh38 |
| NC_000011.9:g.67352697C>G , CM000673.1:g.67352697C>G | GRCh37 |
| NC_000011.8:g.67109273C>G | NCBI36 |
| NG_012075.1:g.6632C>G , LRG_723:g.6632C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000398603.6:c.321C>G | ENSP00000381604.1:p.Leu107= | |
| ENST00000398606.10:c.321C>G MANE Select | ENSP00000381607.3:p.Leu107= | |
| ENST00000646888.1:c.*37C>G | ENSP00000494477.1:n.*37C>G | |
| ENST00000398603.5:c.321C>G | ENSP00000381604.1:p.Leu107= | |
| ENST00000398606.7:c.321C>G | ENSP00000381607.3:p.Leu107= | |
| ENST00000467591.1:n.432C>G | ||
| ENST00000494593.1:n.1116C>G | ||
| ENST00000498765.5:c.384C>G | ||
| NM_000852.3:c.321C>G , LRG_723t1:c.321C>G | NP_000843.1:p.Leu107= | |
| NM_000852.4:c.321C>G MANE Select | NP_000843.1:p.Leu107= |