Linked Data
ClinVar Variation Id:
263868
dbSNP Id:
rs770551687
ExAC:
15:48762956 T / G
gnomAD v2:
15-48762956-T-G
gnomAD v4:
15-48470759-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48470759T>G , CM000677.2:g.48470759T>G | GRCh38 |
| NC_000015.9:g.48762956T>G , CM000677.1:g.48762956T>G | GRCh37 |
| NC_000015.8:g.46550248T>G | NCBI36 |
| NG_008805.2:g.180030A>C , LRG_778:g.180030A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.4337-3A>C | ENSP00000453958.2:n.4337-3A>C | |
| ENST00000674301.2:c.4337-3A>C | ENSP00000501333.2:n.4337-3A>C | |
| ENST00000683268.1:n.304-3A>C | ||
| ENST00000684448.1:n.3011-3A>C | ||
| ENST00000316623.10:c.4337-3A>C MANE Select | ENSP00000325527.5:n.4337-3A>C | |
| ENST00000316623.9:c.4337-3A>C | ENSP00000325527.5:n.4337-3A>C | |
| ENST00000537463.6:c.*100-3A>C | ENSP00000440294.2:n.*100-3A>C | |
| NM_000138.4:c.4337-3A>C , LRG_778t1:c.4337-3A>C | NP_000129.3:n.4337-3A>C | |
| NM_000138.5:c.4337-3A>C MANE Select | NP_000129.3:n.4337-3A>C |