Linked Data
ClinVar Variation Id:
2815333
ClinVar RCV Id:
RCV003627880
MyVariant Identifiers:
chr15:g.89871979T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89328748T>C , CM000677.2:g.89328748T>C | GRCh38 |
| NC_000015.9:g.89871979T>C , CM000677.1:g.89871979T>C | GRCh37 |
| NC_000015.8:g.87672983T>C | NCBI36 |
| NG_008218.1:g.11048A>G | |
| NG_008218.2:g.11048A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636937.2:c.1107A>G | ENSP00000516154.1:p.Leu369= | |
| ENST00000268124.11:c.1107A>G MANE Select | ENSP00000268124.5:p.Leu369= | |
| ENST00000530292.3:c.708A>G | ENSP00000432885.2:p.Leu236= | |
| ENST00000635986.2:c.1107A>G | ENSP00000490653.2:p.Leu369= | |
| ENST00000636774.1:c.1107A>G | ENSP00000489799.1:p.Leu369= | |
| ENST00000637264.1:c.179A>G | ||
| ENST00000666746.1:c.764A>G | ||
| ENST00000672071.1:n.1305A>G | ||
| ENST00000672923.2:n.104A>G | ||
| ENST00000268124.9:c.1107A>G | ENSP00000268124.5:p.Leu369= | |
| ENST00000442287.6:c.1107A>G | ENSP00000399851.2:p.Leu369= | |
| ENST00000631044.2:c.*490A>G | ENSP00000486730.1:n.*490A>G | |
| NM_001126131.1:c.1107A>G | NP_001119603.1:p.Leu369= | |
| NM_002693.2:c.1107A>G | NP_002684.1:p.Leu369= | |
| NM_001126131.2:c.1107A>G | NP_001119603.1:p.Leu369= | |
| NM_002693.3:c.1107A>G MANE Select | NP_002684.1:p.Leu369= |