Linked Data
dbSNP Id:
rs1334186373
gnomAD v4:
21-43169365-C-T
MyVariant Identifiers:
chr21:g.43169365C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.43169365C>T , CM000683.2:g.43169365C>T | GRCh38 |
| NG_009823.1:g.5335C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291554.6:c.189+77C>T MANE Select | ENSP00000291554.2:n.189+77C>T | |
| ENST00000482775.1:n.202+77C>T | ||
| NM_000394.3:c.189+77C>T | NP_000385.1:n.189+77C>T | |
| XR_001755073.1:n.647+1672G>A | ||
| NM_000394.4:c.189+77C>T MANE Select | NP_000385.1:n.189+77C>T |