Linked Data
ClinVar Variation Id:
5641
dbSNP Id:
rs34116584
ExAC:
2:241808314 C / T
gnomAD v2:
2-241808314-C-T
gnomAD v3:
2-240868897-C-T
gnomAD v4:
2-240868897-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240868897C>T , CM000664.2:g.240868897C>T | GRCh38 |
| NC_000002.11:g.241808314C>T , CM000664.1:g.241808314C>T | GRCh37 |
| NC_000002.10:g.241456987C>T | NCBI36 |
| NG_008005.1:g.5153C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307503.4:c.32C>T MANE Select | ENSP00000302620.3:p.Pro11Leu | |
| ENST00000307503.3:c.32C>T | ENSP00000302620.3:p.Pro11Leu | |
| ENST00000472436.1:n.52C>T | ||
| NM_000030.2:c.32C>T | NP_000021.1:p.Pro11Leu | |
| XR_924060.1:n.405+1336G>A | ||
| NM_000030.3:c.32C>T MANE Select | NP_000021.1:p.Pro11Leu |