Linked Data
dbSNP Id:
rs969076482
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.45393740A>T , CM000677.2:g.45393740A>T | GRCh38 |
| NC_000015.9:g.45685938A>T , CM000677.1:g.45685938A>T | GRCh37 |
| NC_000015.8:g.43473230A>T | NCBI36 |
| NG_011674.2:g.13578T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000458245.5:n.640+3182T>A | ||
| ENST00000527933.2:n.512+2427T>A | ||
| ENST00000560538.1:n.338+3182T>A | ||
| ENST00000561148.5:c.-319+3182T>A | ENSP00000453860.1:n.-319+3182T>A | |
| XM_011521450.1:c.31+3182T>A | XP_011519752.1:n.31+3182T>A | |
| NM_001321015.1:c.-395+3182T>A | NP_001307944.1:n.-395+3182T>A | |
| NM_001321015.2:c.-395+3182T>A | NP_001307944.1:n.-395+3182T>A |