Linked Data
dbSNP Id:
rs11989122
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117815600G>T , CM000670.2:g.117815600G>T | GRCh38 |
| NC_000008.10:g.118827839G>T , CM000670.1:g.118827839G>T | GRCh37 |
| NC_000008.9:g.118897020G>T | NCBI36 |
| NG_007455.2:g.301220C>A , LRG_493:g.301220C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000684189.1:n.1100-2639C>A | ||
| ENST00000378204.7:c.1633-2639C>A MANE Select | ENSP00000367446.3:n.1633-2639C>A | |
| ENST00000378204.6:c.1633-2639C>A | ENSP00000367446.2:n.1633-2639C>A | |
| ENST00000437196.1:c.*524-2639C>A | ENSP00000407299.1:n.*524-2639C>A | |
| NM_000127.2:c.1633-2639C>A , LRG_493t1:c.1633-2639C>A | NP_000118.2:n.1633-2639C>A | |
| NM_000127.3:c.1633-2639C>A MANE Select | NP_000118.2:n.1633-2639C>A |