Linked Data
dbSNP Id:
rs559606474
gnomAD v2:
10-1452630-C-T
gnomAD v3:
10-1410435-C-T
gnomAD v4:
10-1410435-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.1410435C>T , CM000672.2:g.1410435C>T | GRCh38 |
| NC_000010.10:g.1452630C>T , CM000672.1:g.1452630C>T | GRCh37 |
| NC_000010.9:g.1442630C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381312.6:c.101-31275G>A MANE Select | ENSP00000370713.1:n.101-31275G>A | |
| ENST00000381312.5:c.101-31275G>A | ENSP00000370713.1:n.101-31275G>A | |
| NM_018702.3:c.101-31275G>A | NP_061172.1:n.101-31275G>A | |
| XR_930468.1:n.449-31275G>A | ||
| NM_018702.4:c.101-31275G>A MANE Select | NP_061172.1:n.101-31275G>A |