Linked Data
ClinVar Variation Id:
1648904
ClinVar RCV Id:
RCV002141433
dbSNP Id:
rs2152067986
MyVariant Identifiers:
chr15:g.89872033G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89328802G>A , CM000677.2:g.89328802G>A | GRCh38 |
| NC_000015.9:g.89872033G>A , CM000677.1:g.89872033G>A | GRCh37 |
| NC_000015.8:g.87673037G>A | NCBI36 |
| NG_008218.1:g.10994C>T | |
| NG_008218.2:g.10994C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636937.2:c.1053C>T | ENSP00000516154.1:p.Ser351= | |
| ENST00000268124.11:c.1053C>T MANE Select | ENSP00000268124.5:p.Ser351= | |
| ENST00000530292.3:c.654C>T | ENSP00000432885.2:p.Ser218= | |
| ENST00000635986.2:c.1053C>T | ENSP00000490653.2:p.Ser351= | |
| ENST00000636774.1:c.1053C>T | ENSP00000489799.1:p.Ser351= | |
| ENST00000637264.1:c.125C>T | ||
| ENST00000666746.1:c.710C>T | ||
| ENST00000672071.1:n.1251C>T | ||
| ENST00000672923.2:n.50C>T | ||
| ENST00000268124.9:c.1053C>T | ENSP00000268124.5:p.Ser351= | |
| ENST00000442287.6:c.1053C>T | ENSP00000399851.2:p.Ser351= | |
| ENST00000631044.2:c.*436C>T | ENSP00000486730.1:n.*436C>T | |
| NM_001126131.1:c.1053C>T | NP_001119603.1:p.Ser351= | |
| NM_002693.2:c.1053C>T | NP_002684.1:p.Ser351= | |
| NM_001126131.2:c.1053C>T | NP_001119603.1:p.Ser351= | |
| NM_002693.3:c.1053C>T MANE Select | NP_002684.1:p.Ser351= |