Linked Data
dbSNP Id:
rs988194208
gnomAD v4:
10-17849773-C-T
MyVariant Identifiers:
chr10:g.17849773C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.17849773C>T , CM000672.2:g.17849773C>T | GRCh38 |
| NG_047011.1:g.45431C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000569591.3:c.1249+9C>T MANE Select | ENSP00000455897.1:n.1249+9C>T | |
| ENST00000569591.2:c.1249+9C>T | ENSP00000455897.1:n.1249+9C>T | |
| NM_002438.3:c.1249+9C>T | NP_002429.1:n.1249+9C>T | |
| NM_002438.4:c.1249+9C>T MANE Select | NP_002429.1:n.1249+9C>T |