Linked Data
dbSNP Id:
rs2135359476
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.72134471C>T , CM000673.2:g.72134471C>T | GRCh38 |
| NC_000011.9:g.71845517C>T , CM000673.1:g.71845517C>T | GRCh37 |
| NC_000011.8:g.71523165C>T | NCBI36 |
| NG_032935.1:g.3747C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622388.4:c.-6-1476C>T | ENSP00000481833.1:n.-6-1476C>T |