Linked Data
dbSNP Id:
rs1569134141
gnomAD v3:
21-44456686-C-T
COSMIC:
COSM4400987
MyVariant Identifiers:
chr21:g.45876569C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44456686C>T , CM000683.2:g.44456686C>T | GRCh38 |
| NC_000021.8:g.45876569C>T , CM000683.1:g.45876569C>T | GRCh37 |
| NC_000021.7:g.44700997C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291592.6:c.42C>T MANE Select | ENSP00000291592.4:p.Val14= | |
| ENST00000291592.5:c.42C>T | ENSP00000291592.4:p.Val14= | |
| NM_030891.4:c.42C>T | NP_112153.1:p.Val14= | |
| NM_030891.5:c.42C>T | NP_112153.1:p.Val14= | |
| NM_030891.6:c.42C>T MANE Select | NP_112153.1:p.Val14= |