Linked Data
ClinVar Variation Id:
1238616
ClinVar RCV Id:
RCV001639019
dbSNP Id:
rs150146676
gnomAD v2:
1-17355012-G-T
gnomAD v3:
1-17028517-G-T
gnomAD v4:
1-17028517-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17028517G>T , CM000663.2:g.17028517G>T | GRCh38 |
| NC_000001.10:g.17355012G>T , CM000663.1:g.17355012G>T | GRCh37 |
| NC_000001.9:g.17227599G>T | NCBI36 |
| NG_012340.1:g.30654C>A , LRG_316:g.30654C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.252+83C>A | ENSP00000481376.2:n.252+83C>A | |
| ENST00000491274.6:c.381+83C>A | ENSP00000480482.2:n.381+83C>A | |
| ENST00000375499.8:c.423+83C>A MANE Select | ENSP00000364649.3:n.423+83C>A | |
| ENST00000375499.7:c.423+83C>A | ENSP00000364649.3:n.423+83C>A | |
| ENST00000463045.2:c.252+83C>A | ENSP00000481376.1:n.252+83C>A | |
| ENST00000475506.1:n.340+83C>A | ||
| ENST00000485515.5:n.357+137C>A | ||
| ENST00000491274.5:c.381+83C>A | ENSP00000480482.1:n.381+83C>A | |
| NM_003000.2:c.423+83C>A , LRG_316t1:c.423+83C>A | NP_002991.2:n.423+83C>A | |
| NM_003000.3:c.423+83C>A MANE Select | NP_002991.2:n.423+83C>A |