Linked Data
dbSNP Id:
rs2113586834
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.22131710T>C , CM000668.2:g.22131710T>C | GRCh38 |
| NC_000006.11:g.22131939T>C , CM000668.1:g.22131939T>C | GRCh37 |
| NC_000006.10:g.22239918T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_015410.1:n.1391+20790T>C | ||
| NR_015410.2:n.1422+20790T>C |