Linked Data
dbSNP Id:
rs1823205517
gnomAD v3:
9-2116088-G-C
gnomAD v4:
9-2116088-G-C
MyVariant Identifiers:
chr9:g.2116088G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.2116088G>C , CM000671.2:g.2116088G>C | GRCh38 |
| NC_000009.11:g.2116088G>C , CM000671.1:g.2116088G>C | GRCh37 |
| NC_000009.10:g.2106088G>C | NCBI36 |
| NG_032162.1:g.105747G>C | |
| NG_032162.2:g.140799G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000704350.1:c.3324+39G>C | ENSP00000515861.1:n.3324+39G>C | |
| ENST00000704352.1:c.1174-45598G>C | ENSP00000515863.1:n.1174-45598G>C | |
| ENST00000704353.1:c.1174-45598G>C | ENSP00000515864.1:n.1174-45598G>C | |
| ENST00000704354.1:c.3668+39G>C | ||
| ENST00000704355.1:c.2048+39G>C | ||
| ENST00000349721.8:c.3684+39G>C MANE Select | ENSP00000265773.5:n.3684+39G>C | |
| ENST00000357248.8:c.3684+39G>C | ENSP00000349788.2:n.3684+39G>C | |
| ENST00000635739.1:n.2352+39G>C | ||
| ENST00000636157.1:n.1291+39G>C | ||
| ENST00000638139.1:n.718+39G>C | ||
| ENST00000349721.7:c.3684+39G>C | ENSP00000265773.5:n.3684+39G>C | |
| ENST00000357248.7:c.3684+39G>C | ENSP00000349788.2:n.3684+39G>C | |
| ENST00000382194.6:c.3684+39G>C | ENSP00000371629.1:n.3684+39G>C | |
| ENST00000382203.5:c.3684+39G>C | ENSP00000371638.1:n.3684+39G>C | |
| ENST00000450198.6:c.3510+39G>C | ENSP00000392081.2:n.3510+39G>C | |
| ENST00000634760.1:c.3684+39G>C | ENSP00000489256.1:n.3684+39G>C | |
| ENST00000634772.1:c.62-3370G>C | ||
| ENST00000634925.1:n.1175+39G>C | ||
| NM_001289396.1:c.3684+39G>C | NP_001276325.1:n.3684+39G>C | |
| NM_001289397.1:c.3510+39G>C | NP_001276326.1:n.3510+39G>C | |
| NM_003070.4:c.3684+39G>C | NP_003061.3:n.3684+39G>C | |
| NM_139045.3:c.3684+39G>C | NP_620614.2:n.3684+39G>C | |
| NM_003070.5:c.3684+39G>C MANE Select | NP_003061.3:n.3684+39G>C | |
| NM_001289397.2:c.3510+39G>C | NP_001276326.1:n.3510+39G>C | |
| NM_139045.4:c.3684+39G>C | NP_620614.2:n.3684+39G>C |