Linked Data
ClinVar Variation Id:
261037
dbSNP Id:
rs3826033
ExAC:
15:91548601 G / A
gnomAD v2:
15-91548601-G-A
gnomAD v3:
15-91005371-G-A
gnomAD v4:
15-91005371-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.91005371G>A , CM000677.2:g.91005371G>A | GRCh38 |
| NC_000015.9:g.91548601G>A , CM000677.1:g.91548601G>A | GRCh37 |
| NC_000015.8:g.89349605G>A | NCBI36 |
| NG_012162.1:g.22233C>T , LRG_884:g.22233C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333371.8:c.1105+9C>T MANE Select | ENSP00000327650.4:n.1105+9C>T | |
| ENST00000643536.1:c.1105+9C>T | ENSP00000494429.1:n.1105+9C>T | |
| ENST00000647331.1:c.1105+9C>T | ENSP00000493953.1:n.1105+9C>T | |
| ENST00000333371.7:c.1105+9C>T | ENSP00000327650.3:n.1105+9C>T | |
| ENST00000535906.1:c.1024+9C>T | ENSP00000444053.1:n.1024+9C>T | |
| ENST00000574755.5:c.*800+9C>T | ENSP00000460413.1:n.*800+9C>T | |
| NM_001289148.1:c.1024+9C>T | NP_001276077.1:n.1024+9C>T | |
| NM_001289149.1:c.832+9C>T | NP_001276078.1:n.832+9C>T | |
| NM_018668.4:c.1105+9C>T , LRG_884t1:c.1105+9C>T | NP_061138.3:n.1105+9C>T | |
| XM_005254884.2:c.1027+9C>T | XP_005254941.1:n.1027+9C>T | |
| XM_005254887.1:c.832+9C>T | XP_005254944.1:n.832+9C>T | |
| XM_005254888.2:c.1105+9C>T | XP_005254945.1:n.1105+9C>T | |
| XM_011521448.1:c.832+9C>T | XP_011519750.1:n.832+9C>T | |
| XM_011521449.1:c.781+9C>T | XP_011519751.1:n.781+9C>T | |
| XM_011521449.2:c.781+9C>T | XP_011519751.1:n.781+9C>T | |
| XM_017022075.2:c.760+9C>T | XP_016877564.1:n.760+9C>T | |
| XM_017022076.1:c.760+9C>T | XP_016877565.1:n.760+9C>T | |
| XR_001751213.2:n.1441+9C>T | ||
| NM_018668.5:c.1105+9C>T MANE Select | NP_061138.3:n.1105+9C>T |