Linked Data
dbSNP Id:
rs1390501330
gnomAD v2:
17-61558046-G-A
gnomAD v3:
17-63480685-G-A
gnomAD v4:
17-63480685-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63480685G>A , CM000679.2:g.63480685G>A | GRCh38 |
| NC_000017.10:g.61558046G>A , CM000679.1:g.61558046G>A | GRCh37 |
| NC_000017.9:g.58911778G>A | NCBI36 |
| NG_011648.1:g.8613G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290866.10:c.847+157G>A MANE Select | ENSP00000290866.4:n.847+157G>A | |
| ENST00000290866.9:c.847+157G>A | ENSP00000290866.4:n.847+157G>A | |
| ENST00000428043.5:c.847+157G>A | ENSP00000397593.2:n.847+157G>A | |
| ENST00000582627.1:c.847+157G>A | ENSP00000462280.1:n.847+157G>A | |
| ENST00000582678.5:c.*246+157G>A | ENSP00000462995.1:n.*246+157G>A | |
| ENST00000584529.5:n.881+157G>A | ||
| NM_000789.3:c.847+157G>A | NP_000780.1:n.847+157G>A | |
| XM_005257110.1:c.298+157G>A | XP_005257167.1:n.298+157G>A | |
| NM_000789.4:c.847+157G>A MANE Select | NP_000780.1:n.847+157G>A | |
| NM_001382700.1:c.374+157G>A | NP_001369629.1:n.374+157G>A | |
| NM_001382701.1:c.-6+157G>A | NP_001369630.1:n.-6+157G>A |