Linked Data
ClinVar Variation Id:
896087
ClinVar RCV Id:
RCV001138542
dbSNP Id:
rs896902158
gnomAD v3:
2-96251509-G-A
gnomAD v4:
2-96251509-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.96251509G>A , CM000664.2:g.96251509G>A | GRCh38 |
| NC_000002.11:g.96917247G>A , CM000664.1:g.96917247G>A | GRCh37 |
| NC_000002.10:g.96280974G>A | NCBI36 |
| NG_027695.1:g.19505C>T , LRG_528:g.19505C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258439.8:c.*2299C>T MANE Select | ENSP00000258439.3:n.*2299C>T | |
| ENST00000258439.7:c.*2299C>T | ENSP00000258439.2:n.*2299C>T | |
| NM_001193304.2:c.*2299C>T | NP_001180233.1:n.*2299C>T | |
| NM_017849.3:c.*2299C>T , LRG_528t1:c.*2299C>T | NP_060319.1:n.*2299C>T | |
| XM_017004450.1:c.*1600C>T | XP_016859939.1:n.*1600C>T | |
| XM_017004452.1:c.*2299C>T | XP_016859941.1:n.*2299C>T | |
| NM_001193304.3:c.*2299C>T | NP_001180233.1:n.*2299C>T | |
| NM_017849.4:c.*2299C>T MANE Select | NP_060319.1:n.*2299C>T |