Linked Data
dbSNP Id:
rs1965967430
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.20353106T>C , CM000678.2:g.20353106T>C | GRCh38 |
| NC_000016.9:g.20364428T>C , CM000678.1:g.20364428T>C | GRCh37 |
| NC_000016.8:g.20271929T>C | NCBI36 |
| NG_008151.1:g.4610A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000570689.5:c.-39-2330A>G | ENSP00000460548.1:n.-39-2330A>G | |
| XM_011545938.1:c.-39-2330A>G | XP_011544240.1:n.-39-2330A>G |