Linked Data
ClinVar Variation Id:
1945236
ClinVar RCV Id:
RCV002640118
dbSNP Id:
rs375991089
ExAC:
2:15358947 C / T
gnomAD v2:
2-15358947-C-T
gnomAD v3:
2-15218823-C-T
gnomAD v4:
2-15218823-C-T
COSMIC:
COSM1400171
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.15218823C>T , CM000664.2:g.15218823C>T | GRCh38 |
| NC_000002.11:g.15358947C>T , CM000664.1:g.15358947C>T | GRCh37 |
| NC_000002.10:g.15276398C>T | NCBI36 |
| NG_032964.1:g.347526G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700061.1:c.4368G>A | ||
| ENST00000700062.1:c.4426+13599G>A | ||
| ENST00000700063.1:c.893G>A | ||
| ENST00000700064.1:c.2238G>A | ||
| ENST00000281513.10:c.6382G>A MANE Select | ENSP00000281513.5:p.Val2128Met | |
| ENST00000281513.9:c.6382G>A | ENSP00000281513.5:p.Val2128Met | |
| ENST00000417461.5:c.512+13599G>A | ENSP00000392421.1:n.512+13599G>A | |
| ENST00000442506.5:c.3525G>A | ||
| NM_015909.3:c.6382G>A | NP_056993.2:p.Val2128Met | |
| NR_052013.2:n.6280+13599G>A | ||
| XM_011510357.1:c.6253G>A | XP_011508659.1:p.Val2085Met | |
| XM_011510358.1:c.6382G>A | XP_011508660.1:p.Val2128Met | |
| XM_011510359.1:c.5743G>A | XP_011508661.1:p.Val1915Met | |
| XM_011510360.1:c.4183G>A | XP_011508662.1:p.Val1395Met | |
| XM_011510361.1:c.4174G>A | XP_011508663.1:p.Val1392Met | |
| XM_011510357.2:c.6253G>A | XP_011508659.1:p.Val2085Met | |
| XM_011510358.2:c.6382G>A | XP_011508660.1:p.Val2128Met | |
| XM_011510360.2:c.4183G>A | XP_011508662.1:p.Val1395Met | |
| XM_011510361.2:c.4174G>A | XP_011508663.1:p.Val1392Met | |
| XM_017004317.1:c.6382G>A | XP_016859806.1:p.Val2128Met | |
| XM_024452961.1:c.5743G>A | XP_024308729.1:p.Val1915Met | |
| NM_015909.4:c.6382G>A MANE Select | NP_056993.2:p.Val2128Met | |
| NR_052013.3:n.6266+13599G>A |