Linked Data
ClinVar Variation Id:
204164
ClinVar RCV Id:
RCV000186371
dbSNP Id:
rs180177219
gnomAD v4:
2-240871347-A-G
PubMed:
PMID:17495019
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240871347A>G , CM000664.2:g.240871347A>G | GRCh38 |
| NC_000002.11:g.241810764A>G , CM000664.1:g.241810764A>G | GRCh37 |
| NC_000002.10:g.241459437A>G | NCBI36 |
| NG_008005.1:g.7603A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.424-2A>G MANE Select | ENSP00000302620.3:n.424-2A>G | |
| ENST00000307503.3:c.424-2A>G | ENSP00000302620.3:n.424-2A>G | |
| ENST00000472436.1:n.444-2A>G | ||
| ENST00000476698.1:n.159A>G | ||
| NM_000030.2:c.424-2A>G | NP_000021.1:n.424-2A>G | |
| NM_000030.3:c.424-2A>G MANE Select | NP_000021.1:n.424-2A>G |