Linked Data
dbSNP Id:
rs1476949230
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68737262T>A , CM000678.2:g.68737262T>A | GRCh38 |
| NC_000016.9:g.68771165T>A , CM000678.1:g.68771165T>A | GRCh37 |
| NC_000016.8:g.67328666T>A | NCBI36 |
| NG_008021.1:g.4971T>A , LRG_301:g.4971T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.9:c.-154T>A | ENSP00000261769.4:n.-154T>A |