Linked Data
dbSNP Id:
rs1810950779
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.104379233C>T , CM000670.2:g.104379233C>T | GRCh38 |
| NC_000008.10:g.105391461C>T , CM000670.1:g.105391461C>T | GRCh37 |
| NC_000008.9:g.105460637C>T | NCBI36 |
| NG_008840.1:g.92817G>A | |
| NG_008840.2:g.92817G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000521601.1:n.328+1951G>A |