Linked Data
dbSNP Id:
rs137958929
gnomAD v3:
11-47235283-C-G
gnomAD v4:
11-47235283-C-G
MyVariant Identifiers:
chr11:g.47256834C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47235283C>G , CM000673.2:g.47235283C>G | GRCh38 |
| NC_000011.9:g.47256834C>G , CM000673.1:g.47256834C>G | GRCh37 |
| NC_000011.8:g.47213410C>G | NCBI36 |
| NG_009365.1:g.25342C>G , LRG_467:g.25342C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256996.9:c.894C>G MANE Select | ENSP00000256996.4:p.Pro298= | |
| ENST00000256996.8:c.894C>G | ENSP00000256996.3:p.Pro298= | |
| ENST00000378600.7:c.457-2554C>G | ENSP00000367863.3:n.457-2554C>G | |
| ENST00000378601.7:c.716C>G | ENSP00000367864.3:p.Pro239Arg | |
| ENST00000378603.7:c.702C>G | ENSP00000367866.3:p.Pro234= | |
| ENST00000612309.4:n.2343C>G | ||
| ENST00000614394.1:n.284C>G | ||
| ENST00000616278.4:c.570C>G | ENSP00000478411.1:n.570C>G | |
| ENST00000617022.4:n.1554-2554C>G | ||
| ENST00000617847.4:c.823C>G | ||
| ENST00000620515.1:n.60C>G | ||
| NM_000107.2:c.894C>G , LRG_467t1:c.894C>G | NP_000098.1:p.Pro298= | |
| NM_001300734.1:c.457-2554C>G | NP_001287663.1:n.457-2554C>G | |
| XR_242780.3:n.884C>G | ||
| XR_242780.4:n.884C>G | ||
| NM_000107.3:c.894C>G MANE Select | NP_000098.1:p.Pro298= | |
| NM_001300734.2:c.457-2554C>G | NP_001287663.1:n.457-2554C>G | |
| NM_001399874.1:c.894C>G | NP_001386803.1:p.Pro298= | |
| NM_001399875.1:c.894C>G | NP_001386804.1:p.Pro298= | |
| NM_001399876.1:c.457-2554C>G | NP_001386805.1:n.457-2554C>G | |
| NM_001399878.1:c.702C>G | NP_001386807.1:p.Pro234= | |
| NR_174610.1:n.1145C>G | ||
| NR_174611.1:n.1123C>G |