Linked Data
dbSNP Id:
rs2142993853
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.79373026C>A , CM000678.2:g.79373026C>A | GRCh38 |
| NC_000016.9:g.79406923C>A , CM000678.1:g.79406923C>A | GRCh37 |
| NC_000016.8:g.77964424C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011523084.1:c.*29-160125G>T | XP_011521386.1:n.*29-160125G>T | |
| XM_024450279.1:c.*29-160125G>T | XP_024306047.1:n.*29-160125G>T | |
| XR_001751902.2:n.3231-160125G>T | ||
| XR_002957802.1:n.3231-160125G>T | ||
| XR_002957803.1:n.3231-160125G>T | ||
| XR_002957804.1:n.3231-160125G>T |