Linked Data
dbSNP Id:
rs212388
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.159069404C>A , CM000668.2:g.159069404C>A | GRCh38 |
| NC_000006.11:g.159490436C>A , CM000668.1:g.159490436C>A | GRCh37 |
| NC_000006.10:g.159410424C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011536288.1:c.324-4466G>T | XP_011534590.1:n.324-4466G>T | |
| XM_011536289.1:c.210-4466G>T | XP_011534591.1:n.210-4466G>T | |
| XM_024446608.1:c.324-4466G>T | XP_024302376.1:n.324-4466G>T | |
| XR_001744430.2:n.2618C>A |