Linked Data
dbSNP Id:
rs1867446023
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67585192G>C , CM000673.2:g.67585192G>C | GRCh38 |
| NC_000011.9:g.67352663G>C , CM000673.1:g.67352663G>C | GRCh37 |
| NC_000011.8:g.67109239G>C | NCBI36 |
| NG_012075.1:g.6598G>C , LRG_723:g.6598G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398603.6:c.287G>C | ENSP00000381604.1:p.Gly96Ala | |
| ENST00000398606.10:c.287G>C MANE Select | ENSP00000381607.3:p.Gly96Ala | |
| ENST00000646888.1:c.*3G>C | ENSP00000494477.1:n.*3G>C | |
| ENST00000398603.5:c.287G>C | ENSP00000381604.1:p.Gly96Ala | |
| ENST00000398606.7:c.287G>C | ENSP00000381607.3:p.Gly96Ala | |
| ENST00000467591.1:n.398G>C | ||
| ENST00000494593.1:n.1082G>C | ||
| ENST00000498765.5:c.350G>C | ||
| NM_000852.3:c.287G>C , LRG_723t1:c.287G>C | NP_000843.1:p.Gly96Ala | |
| NM_000852.4:c.287G>C MANE Select | NP_000843.1:p.Gly96Ala |