Linked Data
dbSNP Id:
rs2095877979
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47332307G>T , CM000673.2:g.47332307G>T | GRCh38 |
| NC_000011.9:g.47353858G>T , CM000673.1:g.47353858G>T | GRCh37 |
| NC_000011.8:g.47310434G>T | NCBI36 |
| NG_007667.1:g.25396C>A , LRG_386:g.25396C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000545968.6:c.3628-49C>A MANE Select | ENSP00000442795.1:n.3628-49C>A | |
| ENST00000256993.8:c.3628-49C>A | ENSP00000256993.5:n.3628-49C>A | |
| ENST00000399249.6:c.3628-49C>A | ENSP00000382193.2:n.3628-49C>A | |
| ENST00000545968.5:c.3628-49C>A | ENSP00000442795.1:n.3628-49C>A | |
| NM_000256.3:c.3628-49C>A , LRG_386t1:c.3628-49C>A MANE Select | NP_000247.2:n.3628-49C>A | |
| XM_011520117.1:c.3610-49C>A | XP_011518419.1:n.3610-49C>A | |
| XM_011520118.1:c.3547-49C>A | XP_011518420.1:n.3547-49C>A |