Linked Data
dbSNP Id:
rs2146049354
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.43551709G>T , CM000681.2:g.43551709G>T | GRCh38 |
| NC_000019.9:g.44055861G>T , CM000681.1:g.44055861G>T | GRCh37 |
| NC_000019.8:g.48747701G>T | NCBI36 |
| NG_033799.1:g.28870C>A , LRG_784:g.28870C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262887.10:c.1083-22C>A MANE Select | ENSP00000262887.5:n.1083-22C>A | |
| ENST00000262887.9:c.1083-22C>A | ENSP00000262887.4:n.1083-22C>A | |
| ENST00000543982.5:c.990-22C>A | ENSP00000443671.1:n.990-22C>A | |
| ENST00000597811.5:c.693-22C>A | ||
| NM_006297.2:c.1083-22C>A , LRG_784t1:c.1083-22C>A | NP_006288.2:n.1083-22C>A | |
| NM_006297.3:c.1083-22C>A MANE Select | NP_006288.2:n.1083-22C>A |