MyVariant.info:
GRCh37
chr18:g.19408950C>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.21828989C>G , CM000680.2:g.21828989C>G | GRCh38 |
| NC_000018.9:g.19408950C>G , CM000680.1:g.19408950C>G | GRCh37 |
| NC_000018.8:g.17662948C>G | NCBI36 |
| NG_033272.2:g.129033C>G , LRG_759:g.129033C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695486.1:n.582+9343C>G (MIB1) | ||
| ENST00000261537.7:c.1829+9343C>G (MIB1) MANE Select | ENSP00000261537.6:n.1829+9343C>G | |
| ENST00000261537.6:c.1829+9343C>G (MIB1) | ENSP00000261537.6:n.1829+9343C>G | |
| ENST00000578646.5:n.1806+9343C>G (MIB1) | ||
| NM_020774.3:c.1829+9343C>G , LRG_759t1:c.1829+9343C>G (MIB1) | NP_065825.1:n.1829+9343C>G | |
| NR_110369.1:n.724G>C (MIR133A1HG) | ||
| XM_011526098.1:c.359+9343C>G (MIB1) | XP_011524400.1:n.359+9343C>G | |
| XM_017025873.1:c.1313+9343C>G (MIB1) | XP_016881362.1:n.1313+9343C>G | |
| NM_020774.4:c.1829+9343C>G (MIB1) MANE Select | NP_065825.1:n.1829+9343C>G |