Linked Data
ClinVar Variation Id:
1696103
dbSNP Id:
rs1016346013
gnomAD v2:
19-17954626-C-T
gnomAD v3:
19-17843817-C-T
gnomAD v4:
19-17843817-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.17843817C>T , CM000681.2:g.17843817C>T | GRCh38 |
| NC_000019.9:g.17954626C>T , CM000681.1:g.17954626C>T | GRCh37 |
| NC_000019.8:g.17815626C>T | NCBI36 |
| NG_007273.1:g.9175G>A , LRG_77:g.9175G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000526008.6:c.268G>A | ENSP00000513006.1:p.Val90Met | |
| ENST00000458235.7:c.268G>A MANE Select | ENSP00000391676.1:p.Val90Met | |
| ENST00000458235.5:c.268G>A | ENSP00000391676.1:p.Val90Met | |
| ENST00000526008.5:n.368G>A | ||
| ENST00000527031.5:n.358G>A | ||
| ENST00000527670.5:c.268G>A | ENSP00000432511.1:p.Val90Met | |
| ENST00000528293.1:n.324-326G>A | ||
| ENST00000534444.1:c.268G>A | ENSP00000436421.1:p.Val90Met | |
| NM_000215.3:c.268G>A , LRG_77t1:c.268G>A | NP_000206.2:p.Val90Met | |
| XM_005259896.2:c.397G>A | XP_005259953.1:p.Val133Met | |
| XM_006722745.2:c.268G>A | XP_006722808.1:p.Val90Met | |
| XM_011527990.1:c.397G>A | XP_011526292.1:p.Val133Met | |
| XM_011527991.1:c.397G>A | XP_011526293.1:p.Val133Met | |
| XR_430137.2:n.407G>A | ||
| XM_005259896.3:c.397G>A | XP_005259953.1:p.Val133Met | |
| XM_011527991.2:c.397G>A | XP_011526293.1:p.Val133Met | |
| NM_000215.4:c.268G>A MANE Select | NP_000206.2:p.Val90Met |