Linked Data
dbSNP Id:
rs1231994876
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147882469G>A , CM000669.2:g.147882469G>A | GRCh38 |
| NC_000007.13:g.147579561G>A , CM000669.1:g.147579561G>A | GRCh37 |
| NC_000007.12:g.147210494G>A | NCBI36 |
| NG_007092.2:g.1771109G>A | |
| NG_007092.3:g.1771469G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361727.8:c.2099-21096G>A MANE Select | ENSP00000354778.3:n.2099-21096G>A | |
| ENST00000636870.1:n.1961-21096G>A | ||
| ENST00000637825.1:n.1582-21096G>A | ||
| ENST00000361727.7:c.2099-21096G>A | ENSP00000354778.3:n.2099-21096G>A | |
| ENST00000455301.2:n.34-21096G>A | ||
| ENST00000627772.2:n.272-21096G>A | ||
| NM_014141.5:c.2099-21096G>A | NP_054860.1:n.2099-21096G>A | |
| XM_006715919.1:c.587-21096G>A | XP_006715982.1:n.587-21096G>A | |
| NM_014141.6:c.2099-21096G>A MANE Select | NP_054860.1:n.2099-21096G>A |