Linked Data
dbSNP Id:
rs212388
gnomAD v2:
6-159490436-C-T
gnomAD v3:
6-159069404-C-T
gnomAD v4:
6-159069404-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.159069404C>T , CM000668.2:g.159069404C>T | GRCh38 |
| NC_000006.11:g.159490436C>T , CM000668.1:g.159490436C>T | GRCh37 |
| NC_000006.10:g.159410424C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XM_011536288.1:c.324-4466G>A | XP_011534590.1:n.324-4466G>A | |
| XM_011536289.1:c.210-4466G>A | XP_011534591.1:n.210-4466G>A | |
| XM_024446608.1:c.324-4466G>A | XP_024302376.1:n.324-4466G>A | |
| XR_001744430.2:n.2618C>T |