Linked Data
dbSNP Id:
rs1304101407
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.41751219C>A , CM000668.2:g.41751219C>A | GRCh38 |
| NC_000006.11:g.41718957C>A , CM000668.1:g.41718957C>A | GRCh37 |
| NC_000006.10:g.41826935C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000415707.1:c.71+2679G>T | ENSP00000399429.1:n.71+2679G>T |