Linked Data
dbSNP Id:
rs1419762398
gnomAD v2:
6-32188614-C-T
gnomAD v3:
6-32220837-C-T
gnomAD v4:
6-32220837-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32220837C>T , CM000668.2:g.32220837C>T | GRCh38 |
| NC_000006.11:g.32188614C>T , CM000668.1:g.32188614C>T | GRCh37 |
| NC_000006.10:g.32296592C>T | NCBI36 |
| NG_028190.1:g.8231G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375023.3:c.841G>A MANE Select | ENSP00000364163.3:p.Val281Ile | |
| ENST00000473562.1:n.970G>A | ||
| NM_004557.3:c.841G>A | NP_004548.3:p.Val281Ile | |
| NR_134949.1:n.980G>A | ||
| NR_134950.1:n.980G>A | ||
| NM_004557.4:c.841G>A MANE Select | NP_004548.3:p.Val281Ile | |
| NR_134949.2:n.980G>A | ||
| NR_134950.2:n.980G>A |