Linked Data
ClinVar Variation Id:
197484
dbSNP Id:
rs148821986
ExAC:
2:238234345 G / A
gnomAD v2:
2-238234345-G-A
gnomAD v3:
2-237325702-G-A
gnomAD v4:
2-237325702-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237325702G>A , CM000664.2:g.237325702G>A | GRCh38 |
| NC_000002.11:g.238234345G>A , CM000664.1:g.238234345G>A | GRCh37 |
| NC_000002.10:g.237899084G>A | NCBI36 |
| NG_008676.1:g.93506C>T , LRG_473:g.93506C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347401.8:c.1732C>T | ||
| ENST00000353578.9:c.8733C>T | ENSP00000315873.4:p.Asp2911= | |
| ENST00000682957.1:c.1478C>T | ||
| ENST00000683348.1:c.217C>T | ENSP00000508058.1:n.217C>T | |
| ENST00000295550.9:c.9351C>T MANE Select | ENSP00000295550.4:p.Asp3117= | |
| ENST00000295550.8:c.9351C>T | ENSP00000295550.4:p.Asp3117= | |
| ENST00000347401.7:c.7527C>T | ENSP00000315609.4:p.Asp2509= | |
| ENST00000353578.8:c.8733C>T | ENSP00000315873.4:p.Asp2911= | |
| ENST00000409809.5:c.8733C>T | ENSP00000386844.1:p.Asp2911= | |
| ENST00000472056.5:c.7530C>T | ENSP00000418285.1:p.Asp2510= | |
| ENST00000473258.1:n.4479C>T | ||
| ENST00000491769.1:n.5793C>T | ||
| NM_004369.3:c.9351C>T , LRG_473t1:c.9351C>T | NP_004360.2:p.Asp3117= | |
| NM_057166.4:c.7530C>T | NP_476507.3:p.Asp2510= | |
| NM_057167.3:c.8733C>T | NP_476508.2:p.Asp2911= | |
| XM_005246065.1:c.8751C>T | XP_005246122.1:p.Asp2917= | |
| XM_005246066.1:c.8130C>T | XP_005246123.1:p.Asp2710= | |
| XM_006712253.1:c.8850C>T | XP_006712316.1:p.Asp2950= | |
| XM_011510574.1:c.9348C>T | XP_011508876.1:p.Asp3116= | |
| XM_011510575.1:c.6945C>T | XP_011508877.1:p.Asp2315= | |
| XM_017003304.1:c.6945C>T | XP_016858793.1:p.Asp2315= | |
| XM_024452684.1:c.8130C>T | XP_024308452.1:p.Asp2710= | |
| NM_004369.4:c.9351C>T MANE Select | NP_004360.2:p.Asp3117= | |
| NM_057166.5:c.7530C>T | NP_476507.3:p.Asp2510= | |
| NM_057167.4:c.8733C>T | NP_476508.2:p.Asp2911= |