Linked Data
dbSNP Id:
rs1645320586
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.53196645G>A , CM000663.2:g.53196645G>A | GRCh38 |
| NC_000001.10:g.53662317G>A , CM000663.1:g.53662317G>A | GRCh37 |
| NC_000001.9:g.53434905G>A | NCBI36 |
| NG_008035.1:g.5217G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371486.3:c.-299G>A | ENSP00000360541.3:n.-299G>A | |
| NM_000098.2:c.-299G>A | NP_000089.1:n.-299G>A | |
| NM_001330589.1:c.-299G>A | NP_001317518.1:n.-299G>A |