Linked Data
ClinVar Variation Id:
1096108
ClinVar RCV Id:
RCV001417243
dbSNP Id:
rs1219136331
MyVariant Identifiers:
chr15:g.68510958G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68218620G>A , CM000677.2:g.68218620G>A | GRCh38 |
| NC_000015.9:g.68510958G>A , CM000677.1:g.68510958G>A | GRCh37 |
| NC_000015.8:g.66298012G>A | NCBI36 |
| NG_008764.2:g.43592C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249806.11:c.114C>T MANE Select | ENSP00000249806.5:p.Ala38= | |
| ENST00000562767.2:c.83+10882C>T | ENSP00000456336.1:n.83+10882C>T | |
| ENST00000563917.2:n.41-4232C>T | ||
| ENST00000565471.6:c.84-8861C>T | ENSP00000457384.1:n.84-8861C>T | |
| ENST00000569336.2:n.23C>T | ||
| ENST00000635747.1:c.*17C>T | ENSP00000490627.1:n.*17C>T | |
| ENST00000636020.1:n.246C>T | ||
| ENST00000636212.1:c.114C>T | ENSP00000489851.1:p.Ala38= | |
| ENST00000636314.1:c.84-4232C>T | ENSP00000490295.1:n.84-4232C>T | |
| ENST00000636876.1:c.*134C>T | ENSP00000489950.1:n.*134C>T | |
| ENST00000637054.1:c.114C>T | ENSP00000490807.1:p.Ala38= | |
| ENST00000637223.1:c.*17C>T | ENSP00000490010.1:n.*17C>T | |
| ENST00000637329.1:c.25C>T | ||
| ENST00000637450.1:c.84-4232C>T | ENSP00000490204.1:n.84-4232C>T | |
| ENST00000637494.1:c.114C>T | ENSP00000490057.1:p.Ala38= | |
| ENST00000637667.1:c.114C>T | ENSP00000489843.1:p.Ala38= | |
| ENST00000637823.1:c.40C>T | ||
| ENST00000637888.1:c.114C>T | ENSP00000490546.1:p.Ala38= | |
| ENST00000638076.1:c.114C>T | ENSP00000490373.1:p.Ala38= | |
| ENST00000638144.1:n.31-4232C>T | ||
| ENST00000249806.9:c.114C>T | ENSP00000249806.5:p.Ala38= | |
| ENST00000538696.5:c.210C>T | ENSP00000445770.1:p.Ala70= | |
| ENST00000562767.1:c.83+10882C>T | ENSP00000456336.1:n.83+10882C>T | |
| ENST00000564752.1:c.114C>T | ENSP00000457822.1:p.Ala38= | |
| ENST00000564846.1:n.546C>T | ||
| ENST00000565471.5:c.84-8861C>T | ENSP00000457384.1:n.84-8861C>T | |
| ENST00000566347.5:c.114C>T | ENSP00000457783.1:p.Ala38= | |
| ENST00000567060.5:c.114C>T | ENSP00000454818.1:p.Ala38= | |
| ENST00000569336.1:n.200C>T | ||
| NM_017882.2:c.114C>T | NP_060352.1:p.Ala38= | |
| XR_931861.1:n.217C>T | ||
| NM_017882.3:c.114C>T MANE Select | NP_060352.1:p.Ala38= |