Linked Data
ClinVar Variation Id:
1531022
ClinVar RCV Id:
RCV002092220
dbSNP Id:
rs2141139457
gnomAD v4:
15-68211852-C-A
MyVariant Identifiers:
chr15:g.68504190C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.68211852C>A , CM000677.2:g.68211852C>A | GRCh38 |
| NC_000015.9:g.68504190C>A , CM000677.1:g.68504190C>A | GRCh37 |
| NC_000015.8:g.66291244C>A | NCBI36 |
| NG_008764.2:g.50360G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249806.11:c.309G>T MANE Select | ENSP00000249806.5:p.Arg103= | |
| ENST00000562767.2:c.84-14224G>T | ENSP00000456336.1:n.84-14224G>T | |
| ENST00000563917.2:n.151G>T | ||
| ENST00000565471.6:c.84-2093G>T | ENSP00000457384.1:n.84-2093G>T | |
| ENST00000635747.1:c.*212G>T | ENSP00000490627.1:n.*212G>T | |
| ENST00000636212.1:c.298-111G>T | ENSP00000489851.1:n.298-111G>T | |
| ENST00000636314.1:c.183-534G>T | ENSP00000490295.1:n.183-534G>T | |
| ENST00000636674.1:n.1292G>T | ||
| ENST00000636964.1:n.1481G>T | ||
| ENST00000637054.1:c.198+6684G>T | ENSP00000490807.1:n.198+6684G>T | |
| ENST00000637223.1:c.*201-534G>T | ENSP00000490010.1:n.*201-534G>T | |
| ENST00000637329.1:c.278G>T | ||
| ENST00000637450.1:c.194G>T | ENSP00000490204.1:p.Gly65Val | |
| ENST00000637494.1:c.199-534G>T | ENSP00000490057.1:n.199-534G>T | |
| ENST00000637667.1:c.210G>T | ENSP00000489843.1:p.Arg70= | |
| ENST00000637823.1:c.224-209G>T | ||
| ENST00000637888.1:c.198+6684G>T | ENSP00000490546.1:n.198+6684G>T | |
| ENST00000638076.1:c.309G>T | ENSP00000490373.1:p.Arg103= | |
| ENST00000638144.1:n.130-534G>T | ||
| ENST00000646164.1:c.38+6684G>T | ||
| ENST00000249806.9:c.309G>T | ENSP00000249806.5:p.Arg103= | |
| ENST00000538696.5:c.405G>T | ENSP00000445770.1:p.Arg135= | |
| ENST00000562767.1:c.84-14224G>T | ENSP00000456336.1:n.84-14224G>T | |
| ENST00000563917.1:n.90G>T | ||
| ENST00000564752.1:c.309G>T | ENSP00000457822.1:p.Arg103= | |
| ENST00000565471.5:c.84-2093G>T | ENSP00000457384.1:n.84-2093G>T | |
| ENST00000566347.5:c.298-534G>T | ENSP00000457783.1:n.298-534G>T | |
| ENST00000567060.5:c.298-2132G>T | ENSP00000454818.1:n.298-2132G>T | |
| NM_017882.2:c.309G>T | NP_060352.1:p.Arg103= | |
| XR_931861.1:n.412G>T | ||
| NM_017882.3:c.309G>T MANE Select | NP_060352.1:p.Arg103= |