Linked Data
ClinVar Variation Id:
97583
ClinVar RCV Id:
RCV003764775
dbSNP Id:
rs104895354
ExAC:
12:110019197 C / T
gnomAD v2:
12-110019197-C-T
gnomAD v3:
12-109581392-C-T
gnomAD v4:
12-109581392-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.109581392C>T , CM000674.2:g.109581392C>T | GRCh38 |
| NC_000012.11:g.110019197C>T , CM000674.1:g.110019197C>T | GRCh37 |
| NC_000012.10:g.108503580C>T | NCBI36 |
| NG_007702.1:g.12698C>T , LRG_156:g.12698C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000539696.6:c.-92+7519C>T | ENSP00000439134.1:n.-92+7519C>T | |
| ENST00000546277.6:c.372-3C>T | ENSP00000438153.2:n.372-3C>T | |
| ENST00000636529.2:n.79-4630C>T | ||
| ENST00000697195.1:c.*136-3C>T | ENSP00000513181.1:n.*136-3C>T | |
| ENST00000697196.1:c.372-3C>T | ENSP00000513182.1:n.372-3C>T | |
| ENST00000228510.8:c.372-3C>T MANE Select | ENSP00000228510.3:n.372-3C>T | |
| ENST00000636529.1:c.65-4630C>T | ||
| ENST00000636996.1:c.220-3C>T | ||
| ENST00000228510.7:c.372-3C>T | ENSP00000228510.3:n.372-3C>T | |
| ENST00000392727.7:c.371+1446C>T | ENSP00000376487.3:n.371+1446C>T | |
| ENST00000447878.6:c.227-4630C>T | ENSP00000415555.2:n.227-4630C>T | |
| ENST00000535044.1:n.472-4630C>T | ||
| ENST00000537237.5:c.*136-3C>T | ENSP00000445382.1:n.*136-3C>T | |
| ENST00000539335.5:c.372-3C>T | ENSP00000440379.1:n.372-3C>T | |
| ENST00000539575.4:c.372-3C>T | ENSP00000443551.2:n.372-3C>T | |
| ENST00000539696.5:c.-92+7519C>T | ENSP00000439134.1:n.-92+7519C>T | |
| ENST00000545774.5:c.227-4630C>T | ENSP00000443978.1:n.227-4630C>T | |
| ENST00000546277.5:c.372-3C>T | ENSP00000438153.1:n.372-3C>T | |
| ENST00000625889.2:c.371+1446C>T | ENSP00000486846.1:n.371+1446C>T | |
| ENST00000629016.2:c.227-4630C>T | ENSP00000486804.1:n.227-4630C>T | |
| NM_000431.3:c.372-3C>T | NP_000422.1:n.372-3C>T | |
| NM_001114185.2:c.372-3C>T | NP_001107657.1:n.372-3C>T | |
| NM_001301182.1:c.371+1446C>T | NP_001288111.1:n.371+1446C>T | |
| XM_011538372.1:c.372-3C>T | XP_011536674.1:n.372-3C>T | |
| XM_017019313.2:c.371+1446C>T | XP_016874802.1:n.371+1446C>T | |
| XM_017019314.1:c.372-3C>T | XP_016874803.1:n.372-3C>T | |
| XM_024448982.1:c.372-3C>T | XP_024304750.1:n.372-3C>T | |
| NM_000431.4:c.372-3C>T MANE Select | NP_000422.1:n.372-3C>T | |
| NM_001114185.3:c.372-3C>T | NP_001107657.1:n.372-3C>T | |
| NM_001301182.2:c.371+1446C>T | NP_001288111.1:n.371+1446C>T |