Linked Data
dbSNP Id:
rs1940801143
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21174945A>C , CM000674.2:g.21174945A>C | GRCh38 |
| NC_000012.11:g.21327879A>C , CM000674.1:g.21327879A>C | GRCh37 |
| NC_000012.10:g.21219146A>C | NCBI36 |
| NG_011745.1:g.48752A>C , LRG_1022:g.48752A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.359+236A>C MANE Select | ENSP00000256958.2:n.359+236A>C | |
| ENST00000256958.2:c.359+236A>C | ENSP00000256958.2:n.359+236A>C | |
| ENST00000543498.5:c.426-1831A>C | ||
| NM_006446.4:c.359+236A>C , LRG_1022t1:c.359+236A>C | NP_006437.3:n.359+236A>C | |
| NM_006446.5:c.359+236A>C MANE Select | NP_006437.3:n.359+236A>C |