Linked Data
dbSNP Id:
rs1812944084
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.58968519G>C , CM000670.2:g.58968519G>C | GRCh38 |
| NC_000008.10:g.59881078G>C , CM000670.1:g.59881078G>C | GRCh37 |
| NC_000008.9:g.60043632G>C | NCBI36 |
| NG_011993.1:g.155690C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361421.2:c.103-8511C>G MANE Select | ENSP00000354842.1:n.103-8511C>G | |
| ENST00000361421.1:c.103-8511C>G | ENSP00000354842.1:n.103-8511C>G | |
| NM_014729.2:c.103-8511C>G | NP_055544.1:n.103-8511C>G | |
| XM_017014085.1:c.103-28975C>G | XP_016869574.1:n.103-28975C>G | |
| NM_014729.3:c.103-8511C>G MANE Select | NP_055544.1:n.103-8511C>G |