Linked Data
ClinVar Variation Id:
840058
ClinVar RCV Id:
RCV001041958
dbSNP Id:
rs1211135006
gnomAD v3:
17-80089776-G-A
gnomAD v4:
17-80089776-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80089776G>A , CM000679.2:g.80089776G>A | GRCh38 |
| NC_000017.10:g.78063575G>A , CM000679.1:g.78063575G>A | GRCh37 |
| NC_000017.9:g.75678170G>A | NCBI36 |
| NG_029761.1:g.58145G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000397545.9:c.2724G>A MANE Select | ENSP00000380679.4:p.Met908Ile | |
| ENST00000374877.7:c.2724G>A | ENSP00000364011.3:p.Met908Ile | |
| ENST00000397545.8:c.2724G>A | ENSP00000380679.4:p.Met908Ile | |
| ENST00000572253.5:n.2975G>A | ||
| ENST00000573903.1:n.386G>A | ||
| ENST00000574799.5:n.2261G>A | ||
| ENST00000575431.1:n.368G>A | ||
| NM_001243342.1:c.2724G>A | NP_001230271.1:p.Met908Ile | |
| NM_017950.3:c.2724G>A | NP_060420.2:p.Met908Ile | |
| XM_011524963.1:c.2634G>A | XP_011523265.1:p.Met878Ile | |
| XM_011524964.1:c.1545G>A | XP_011523266.1:p.Met515Ile | |
| XR_934495.1:n.2842G>A | ||
| XM_011524963.3:c.2634G>A | XP_011523265.1:p.Met878Ile | |
| XM_011524964.3:c.1545G>A | XP_011523266.1:p.Met515Ile | |
| XM_024450821.1:c.2634G>A | XP_024306589.1:p.Met878Ile | |
| XR_934495.2:n.2842G>A | ||
| NM_017950.4:c.2724G>A MANE Select | NP_060420.2:p.Met908Ile | |
| NM_001243342.2:c.2724G>A | NP_001230271.1:p.Met908Ile |