Linked Data
dbSNP Id:
rs1679659368
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.135845754G>A , CM000664.2:g.135845754G>A | GRCh38 |
| NC_000002.11:g.136603324G>A , CM000664.1:g.136603324G>A | GRCh37 |
| NC_000002.10:g.136319794G>A | NCBI36 |
| NG_008104.2:g.14416C>T , LRG_338:g.14416C>T | |
| NG_008958.1:g.35688C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264156.3:c.2209+483C>T MANE Select | ENSP00000264156.2:n.2209+483C>T | |
| ENST00000264156.2:c.2209+483C>T | ENSP00000264156.2:n.2209+483C>T | |
| ENST00000492091.1:n.635+483C>T | ||
| NM_005915.5:c.2209+483C>T | NP_005906.2:n.2209+483C>T | |
| NM_005915.6:c.2209+483C>T MANE Select | NP_005906.2:n.2209+483C>T |