Linked Data
ClinVar Variation Id:
281372
dbSNP Id:
rs373150395
ExAC:
17:62025363 C / T
gnomAD v2:
17-62025363-C-T
gnomAD v3:
17-63948003-C-T
gnomAD v4:
17-63948003-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63948003C>T , CM000679.2:g.63948003C>T | GRCh38 |
| NC_000017.10:g.62025363C>T , CM000679.1:g.62025363C>T | GRCh37 |
| NC_000017.9:g.59379095C>T | NCBI36 |
| NG_011699.1:g.29916G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000435607.3:c.3205G>A MANE Select | ENSP00000396320.1:p.Asp1069Asn | |
| ENST00000578147.5:c.3205G>A | ENSP00000463963.1:p.Asp1069Asn | |
| ENST00000584310.1:n.528G>A | ||
| NM_000334.4:c.3205G>A MANE Select | NP_000325.4:p.Asp1069Asn | |
| XM_005257566.3:c.3205G>A | XP_005257623.1:p.Asp1069Asn |