Linked Data
ClinVar Variation Id:
1624658
ClinVar RCV Id:
RCV002106262
dbSNP Id:
rs776061925
ExAC:
2:241808578 C / T
gnomAD v2:
2-241808578-C-T
gnomAD v3:
2-240869161-C-T
gnomAD v4:
2-240869161-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869161C>T , CM000664.2:g.240869161C>T | GRCh38 |
| NC_000002.11:g.241808578C>T , CM000664.1:g.241808578C>T | GRCh37 |
| NC_000002.10:g.241457251C>T | NCBI36 |
| NG_008005.1:g.5417C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.166-9C>T MANE Select | ENSP00000302620.3:n.166-9C>T | |
| ENST00000307503.3:c.166-9C>T | ENSP00000302620.3:n.166-9C>T | |
| ENST00000472436.1:n.186-9C>T | ||
| NM_000030.2:c.166-9C>T | NP_000021.1:n.166-9C>T | |
| XR_924060.1:n.405+1072G>A | ||
| NM_000030.3:c.166-9C>T MANE Select | NP_000021.1:n.166-9C>T |