Linked Data
ClinVar Variation Id:
672129
ClinVar RCV Id:
RCV000831349
dbSNP Id:
rs3778337
gnomAD v2:
6-7565885-G-A
gnomAD v3:
6-7565652-G-A
gnomAD v4:
6-7565652-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7565652G>A , CM000668.2:g.7565652G>A | GRCh38 |
| NC_000006.11:g.7565885G>A , CM000668.1:g.7565885G>A | GRCh37 |
| NC_000006.10:g.7510884G>A | NCBI36 |
| NG_008803.1:g.29016G>A , LRG_423:g.29016G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710359.1:c.939+132G>A | ENSP00000518230.1:n.939+132G>A | |
| ENST00000682228.1:n.263+132G>A | ||
| ENST00000379802.8:c.939+132G>A MANE Select | ENSP00000369129.3:n.939+132G>A | |
| ENST00000379802.7:c.939+132G>A | ENSP00000369129.3:n.939+132G>A | |
| ENST00000418664.2:c.939+132G>A | ENSP00000396591.2:n.939+132G>A | |
| ENST00000506617.1:n.589G>A | ||
| NM_001008844.1:c.939+132G>A | NP_001008844.1:n.939+132G>A | |
| NM_004415.2:c.939+132G>A , LRG_423t1:c.939+132G>A | NP_004406.2:n.939+132G>A | |
| XM_011514323.1:c.939+132G>A | XP_011512625.1:n.939+132G>A | |
| NM_001008844.2:c.939+132G>A | NP_001008844.1:n.939+132G>A | |
| NM_001319034.1:c.939+132G>A | NP_001305963.1:n.939+132G>A | |
| NM_004415.3:c.939+132G>A | NP_004406.2:n.939+132G>A | |
| NM_004415.4:c.939+132G>A MANE Select | NP_004406.2:n.939+132G>A | |
| NM_001008844.3:c.939+132G>A | NP_001008844.1:n.939+132G>A | |
| NM_001319034.2:c.939+132G>A | NP_001305963.1:n.939+132G>A |