Linked Data
ClinVar Variation Id:
204162
ClinVar RCV Id:
RCV000186369
dbSNP Id:
rs180177158
PubMed:
PMID:19479957
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240878151G>A , CM000664.2:g.240878151G>A | GRCh38 |
| NC_000002.11:g.241817568G>A , CM000664.1:g.241817568G>A | GRCh37 |
| NC_000002.10:g.241466241G>A | NCBI36 |
| NG_008005.1:g.14407G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.1071+1G>A MANE Select | ENSP00000302620.3:n.1071+1G>A | |
| ENST00000307503.3:c.1071+1G>A | ENSP00000302620.3:n.1071+1G>A | |
| ENST00000470255.1:n.849+1G>A | ||
| NM_000030.2:c.1071+1G>A | NP_000021.1:n.1071+1G>A | |
| NM_000030.3:c.1071+1G>A MANE Select | NP_000021.1:n.1071+1G>A |