Linked Data
ClinVar Variation Id:
451667
dbSNP Id:
rs374493032
ExAC:
2:238277674 C / T
gnomAD v2:
2-238277674-C-T
gnomAD v3:
2-237369031-C-T
gnomAD v4:
2-237369031-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237369031C>T , CM000664.2:g.237369031C>T | GRCh38 |
| NC_000002.11:g.238277674C>T , CM000664.1:g.238277674C>T | GRCh37 |
| NC_000002.10:g.237942413C>T | NCBI36 |
| NG_008676.1:g.50177G>A , LRG_473:g.50177G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000353578.9:c.3814G>A | ENSP00000315873.4:p.Val1272Met | |
| ENST00000684597.1:c.117-355G>A | ||
| ENST00000295550.9:c.4432G>A MANE Select | ENSP00000295550.4:p.Val1478Met | |
| ENST00000295550.8:c.4432G>A | ENSP00000295550.4:p.Val1478Met | |
| ENST00000347401.7:c.2611G>A | ENSP00000315609.4:p.Val871Met | |
| ENST00000353578.8:c.3814G>A | ENSP00000315873.4:p.Val1272Met | |
| ENST00000409809.5:c.3814G>A | ENSP00000386844.1:p.Val1272Met | |
| ENST00000472056.5:c.2611G>A | ENSP00000418285.1:p.Val871Met | |
| NM_004369.3:c.4432G>A , LRG_473t1:c.4432G>A | NP_004360.2:p.Val1478Met | |
| NM_057166.4:c.2611G>A | NP_476507.3:p.Val871Met | |
| NM_057167.3:c.3814G>A | NP_476508.2:p.Val1272Met | |
| XM_005246065.1:c.3832G>A | XP_005246122.1:p.Val1278Met | |
| XM_005246066.1:c.3211G>A | XP_005246123.1:p.Val1071Met | |
| XM_006712253.1:c.4286-355G>A | XP_006712316.1:n.4286-355G>A | |
| XM_011510574.1:c.4429G>A | XP_011508876.1:p.Val1477Met | |
| XM_011510575.1:c.2026G>A | XP_011508877.1:p.Val676Met | |
| XM_017003304.1:c.2026G>A | XP_016858793.1:p.Val676Met | |
| XM_024452684.1:c.3211G>A | XP_024308452.1:p.Val1071Met | |
| NM_004369.4:c.4432G>A MANE Select | NP_004360.2:p.Val1478Met | |
| NM_057166.5:c.2611G>A | NP_476507.3:p.Val871Met | |
| NM_057167.4:c.3814G>A | NP_476508.2:p.Val1272Met |