Linked Data
ClinVar Variation Id:
321849
dbSNP Id:
rs149070440
gnomAD v2:
17-15133322-C-T
gnomAD v3:
17-15230005-C-T
gnomAD v4:
17-15230005-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.15230005C>T , CM000679.2:g.15230005C>T | GRCh38 |
| NC_000017.10:g.15133322C>T , CM000679.1:g.15133322C>T | GRCh37 |
| NC_000017.9:g.15074047C>T | NCBI36 |
| NG_007949.1:g.40323G>A , LRG_263:g.40323G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000312280.9:c.*912G>A MANE Select | ENSP00000308937.3:n.*912G>A | |
| ENST00000395936.7:c.*1104G>A | ENSP00000379268.1:n.*1104G>A | |
| ENST00000395938.7:c.*730G>A | ENSP00000379269.3:n.*730G>A | |
| ENST00000494511.7:c.*912G>A | ENSP00000462782.2:n.*912G>A | |
| ENST00000580584.3:c.*912G>A | ENSP00000464468.3:n.*912G>A | |
| ENST00000612492.5:c.*912G>A | ENSP00000484631.1:n.*912G>A | |
| ENST00000643451.2:c.*1250G>A | ENSP00000494628.1:n.*1250G>A | |
| ENST00000644020.1:c.*1104G>A | ENSP00000496522.1:n.*1104G>A | |
| ENST00000646419.2:c.*1104G>A | ENSP00000494871.1:n.*1104G>A | |
| ENST00000674651.1:c.*912G>A | ENSP00000501727.1:n.*912G>A | |
| ENST00000674673.1:c.*912G>A | ENSP00000501804.1:n.*912G>A | |
| ENST00000674707.1:c.*912G>A | ENSP00000502250.1:n.*912G>A | |
| ENST00000674871.1:n.1411G>A | ||
| ENST00000674947.1:c.*730G>A | ENSP00000501580.1:n.*730G>A | |
| ENST00000675551.1:c.*1064G>A | ENSP00000501945.1:n.*1064G>A | |
| ENST00000675808.1:c.*912G>A | ENSP00000502310.1:n.*912G>A | |
| ENST00000675819.1:c.*912G>A | ENSP00000502018.1:n.*912G>A | |
| ENST00000675854.1:c.*912G>A | ENSP00000502324.1:n.*912G>A | |
| ENST00000675950.1:c.*912G>A | ENSP00000501546.1:n.*912G>A | |
| ENST00000676002.1:n.1388G>A | ||
| ENST00000676161.1:c.*912G>A | ENSP00000501766.1:n.*912G>A | |
| ENST00000676221.1:c.*912G>A | ENSP00000502601.1:n.*912G>A | |
| ENST00000676329.1:c.*912G>A | ENSP00000501698.1:n.*912G>A | |
| ENST00000312280.7:c.*912G>A | ENSP00000308937.3:n.*912G>A | |
| ENST00000395938.6:c.*912G>A | ENSP00000379269.2:n.*912G>A | |
| ENST00000612492.4:c.*912G>A | ENSP00000484631.1:n.*912G>A | |
| NM_000304.3:c.*912G>A | NP_000295.1:n.*912G>A | |
| NM_001281455.1:c.*912G>A | NP_001268384.1:n.*912G>A | |
| NM_001281456.1:c.*912G>A | NP_001268385.1:n.*912G>A | |
| NM_153321.2:c.*912G>A | NP_696996.1:n.*912G>A | |
| NM_153322.2:c.*912G>A | NP_696997.1:n.*912G>A | |
| NR_104017.1:n.1521G>A | ||
| NR_104018.1:n.1421G>A | ||
| NM_000304.4:c.*912G>A MANE Select | NP_000295.1:n.*912G>A | |
| NM_001281456.2:c.*912G>A | NP_001268385.1:n.*912G>A | |
| NM_153321.3:c.*912G>A | NP_696996.1:n.*912G>A | |
| NM_153322.3:c.*912G>A | NP_696997.1:n.*912G>A | |
| NR_104017.2:n.1490G>A | ||
| NR_104018.2:n.1390G>A | ||
| NM_001281455.2:c.*912G>A | NP_001268384.1:n.*912G>A |