Linked Data
ClinVar Variation Id:
204156
ClinVar RCV Id:
RCV000186363
dbSNP Id:
rs180177256
PubMed:
PMID:15963748
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240874067G>C , CM000664.2:g.240874067G>C | GRCh38 |
| NC_000002.11:g.241813484G>C , CM000664.1:g.241813484G>C | GRCh37 |
| NC_000002.10:g.241462157G>C | NCBI36 |
| NG_008005.1:g.10323G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.680+5G>C MANE Select | ENSP00000302620.3:n.680+5G>C | |
| ENST00000307503.3:c.680+5G>C | ENSP00000302620.3:n.680+5G>C | |
| ENST00000476698.1:n.332+1018G>C | ||
| NM_000030.2:c.680+5G>C | NP_000021.1:n.680+5G>C | |
| NM_000030.3:c.680+5G>C MANE Select | NP_000021.1:n.680+5G>C |