Linked Data
ClinVar Variation Id:
178353
dbSNP Id:
rs142356935
ExAC:
5:89910839 A / G
gnomAD v2:
5-89910839-A-G
gnomAD v3:
5-90615022-A-G
gnomAD v4:
5-90615022-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.90615022A>G , CM000667.2:g.90615022A>G | GRCh38 |
| NC_000005.9:g.89910839A>G , CM000667.1:g.89910839A>G | GRCh37 |
| NC_000005.8:g.89946595A>G | NCBI36 |
| NG_007083.1:g.61223A>G | |
| NG_007083.2:g.90679A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000405460.9:c.207+3A>G MANE Select | ENSP00000384582.2:n.207+3A>G | |
| ENST00000638316.1:n.417+3A>G | ||
| ENST00000640109.1:n.303+3A>G | ||
| ENST00000640281.1:n.266+3A>G | ||
| ENST00000405460.6:c.207+3A>G | ENSP00000384582.2:n.207+3A>G | |
| ENST00000508842.5:c.219+3A>G | ENSP00000425936.1:n.219+3A>G | |
| NM_032119.3:c.207+3A>G | NP_115495.3:n.207+3A>G | |
| NR_003149.1:n.303+3A>G | ||
| XM_011543675.1:c.207+3A>G | XP_011541977.1:n.207+3A>G | |
| XM_011543676.1:c.207+3A>G | XP_011541978.1:n.207+3A>G | |
| XM_011543678.1:c.207+3A>G | XP_011541980.1:n.207+3A>G | |
| XM_011543679.1:c.207+3A>G | XP_011541981.1:n.207+3A>G | |
| NM_032119.4:c.207+3A>G MANE Select | NP_115495.3:n.207+3A>G | |
| XM_017009963.2:c.207+3A>G | XP_016865452.1:n.207+3A>G | |
| XM_017009964.2:c.207+3A>G | XP_016865453.1:n.207+3A>G | |
| XM_017009965.1:c.204+3A>G | XP_016865454.1:n.204+3A>G | |
| XM_017009966.2:c.207+3A>G | XP_016865455.1:n.207+3A>G | |
| XM_017009967.1:c.207+3A>G | XP_016865456.1:n.207+3A>G | |
| XM_017009968.2:c.207+3A>G | XP_016865457.1:n.207+3A>G | |
| XM_017009969.2:c.207+3A>G | XP_016865458.1:n.207+3A>G | |
| XM_017009970.2:c.207+3A>G | XP_016865459.1:n.207+3A>G | |
| XM_017009971.2:c.207+3A>G | XP_016865460.1:n.207+3A>G | |
| XM_017009974.2:c.207+3A>G | XP_016865463.1:n.207+3A>G | |
| NR_003149.2:n.306+3A>G |