Linked Data
dbSNP Id:
rs1810952213
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.104379282A>G , CM000670.2:g.104379282A>G | GRCh38 |
| NC_000008.10:g.105391510A>G , CM000670.1:g.105391510A>G | GRCh37 |
| NC_000008.9:g.105460686A>G | NCBI36 |
| NG_008840.1:g.92768T>C | |
| NG_008840.2:g.92768T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000521601.1:n.328+1902T>C |