Linked Data
dbSNP Id:
rs1597063997
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1985887C>A , CM000678.2:g.1985887C>A | GRCh38 |
| NC_000016.9:g.2035888C>A , CM000678.1:g.2035888C>A | GRCh37 |
| NC_000016.8:g.1975889C>A | NCBI36 |
| NG_016288.1:g.6739C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000567719.2:c.252C>A | ENSP00000455885.1:p.Asp84Glu | |
| ENST00000248114.7:c.477C>A MANE Select | ENSP00000248114.6:p.Asp159Glu | |
| ENST00000248114.6:c.477C>A | ENSP00000248114.6:p.Asp159Glu | |
| ENST00000565658.1:n.634C>A | ||
| ENST00000567719.1:c.252C>A | ENSP00000455885.1:p.Asp84Glu | |
| ENST00000569451.1:c.280C>A | ENSP00000456432.1:p.His94Asn | |
| NM_005262.2:c.477C>A | NP_005253.3:p.Asp159Glu | |
| NM_005262.3:c.477C>A MANE Select | NP_005253.3:p.Asp159Glu |