Linked Data
dbSNP Id:
rs926572199
gnomAD v3:
9-93953907-G-A
gnomAD v4:
9-93953907-G-A
MyVariant Identifiers:
chr9:g.93953907G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.93953907G>A , CM000671.2:g.93953907G>A | GRCh38 |
| NC_000009.11:g.96716189G>A , CM000671.1:g.96716189G>A | GRCh37 |
| NC_000009.10:g.95756010G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253968.11:c.224-720C>T MANE Select | ENSP00000253968.5:n.224-720C>T | |
| ENST00000253968.10:c.224-720C>T | ENSP00000253968.5:n.224-720C>T | |
| NM_021570.3:c.224-720C>T | NP_067545.3:n.224-720C>T | |
| NM_021570.4:c.224-720C>T MANE Select | NP_067545.3:n.224-720C>T |