Linked Data
dbSNP Id:
rs1946698267
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.47908774T>C , CM000674.2:g.47908774T>C | GRCh38 |
| NC_000012.11:g.48302557T>C , CM000674.1:g.48302557T>C | GRCh37 |
| NC_000012.10:g.46588824T>C | NCBI36 |
| NG_008731.1:g.1258A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395324.6:c.-83-26000A>G | ENSP00000378734.2:n.-83-26000A>G |