Linked Data
ClinVar Variation Id:
361199
ClinVar RCV Id:
RCV000325699
dbSNP Id:
rs886062573
gnomAD v4:
8-10606796-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.10606796G>T , CM000670.2:g.10606796G>T | GRCh38 |
| NC_000008.10:g.10464306G>T , CM000670.1:g.10464306G>T | GRCh37 |
| NC_000008.9:g.10501716G>T | NCBI36 |
| NG_028035.1:g.53312C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382483.4:c.*99C>A MANE Select | ENSP00000371923.3:n.*99C>A | |
| ENST00000382483.3:c.*99C>A | ENSP00000371923.3:n.*99C>A | |
| NM_178857.5:c.*99C>A | NP_849188.4:n.*99C>A | |
| NM_178857.6:c.*99C>A MANE Select | NP_849188.4:n.*99C>A |