Linked Data
ClinVar Variation Id:
502789
dbSNP Id:
rs758218388
ExAC:
6:42946522 G / A
gnomAD v2:
6-42946522-G-A
gnomAD v3:
6-42978784-G-A
gnomAD v4:
6-42978784-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42978784G>A , CM000668.2:g.42978784G>A | GRCh38 |
| NC_000006.11:g.42946522G>A , CM000668.1:g.42946522G>A | GRCh37 |
| NC_000006.10:g.43054500G>A | NCBI36 |
| NG_008370.1:g.5460C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304611.13:c.367C>T MANE Select | ENSP00000303511.8:p.Leu123= | |
| ENST00000244546.4:c.367C>T | ENSP00000244546.4:p.Leu123= | |
| ENST00000304611.12:c.367C>T | ENSP00000303511.8:p.Leu123= | |
| NM_000287.3:c.367C>T | NP_000278.3:p.Leu123= | |
| NM_001316313.1:c.367C>T | NP_001303242.1:p.Leu123= | |
| NR_133009.1:n.460C>T | ||
| XM_011514661.1:c.367C>T | XP_011512963.1:p.Leu123= | |
| XR_926246.1:n.460C>T | ||
| XM_011514661.2:c.367C>T | XP_011512963.1:p.Leu123= | |
| XR_001743466.2:n.1441C>T | ||
| NM_000287.4:c.367C>T MANE Select | NP_000278.3:p.Leu123= | |
| NM_001316313.2:c.367C>T | NP_001303242.1:p.Leu123= | |
| NR_133009.2:n.398C>T |