Linked Data
ClinVar Variation Id:
214149
dbSNP Id:
rs748318386
ExAC:
9:93983106 G / A
gnomAD v2:
9-93983106-G-A
gnomAD v3:
9-91220824-G-A
gnomAD v4:
9-91220824-G-A
COSMIC:
COSM238917
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.91220824G>A , CM000671.2:g.91220824G>A | GRCh38 |
| NC_000009.11:g.93983106G>A , CM000671.1:g.93983106G>A | GRCh37 |
| NC_000009.10:g.93022927G>A | NCBI36 |
| NG_008017.1:g.146101C>T , LRG_449:g.146101C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375731.9:c.824C>T MANE Select | ENSP00000364883.5:p.Ala275Val | |
| ENST00000303617.5:c.737C>T | ENSP00000307334.5:p.Ala246Val | |
| ENST00000375731.8:c.824C>T | ENSP00000364883.4:p.Ala275Val | |
| ENST00000473695.1:n.96C>T | ||
| NM_001306190.1:c.737C>T | NP_001293119.1:p.Ala246Val | |
| NM_001698.2:c.824C>T , LRG_449t1:c.824C>T | NP_001689.1:p.Ala275Val | |
| XM_005252066.2:c.854C>T | XP_005252123.1:p.Ala285Val | |
| XM_005252067.3:c.854C>T | XP_005252124.1:p.Ala285Val | |
| XM_005252069.3:c.854C>T | XP_005252126.1:p.Ala285Val | |
| XM_005252073.2:c.362C>T | XP_005252130.1:p.Ala121Val | |
| XM_006717150.2:c.767C>T | XP_006717213.1:p.Ala256Val | |
| XM_011518801.1:c.500C>T | XP_011517103.1:p.Ala167Val | |
| XM_011518802.1:c.497C>T | XP_011517104.1:p.Ala166Val | |
| NM_001351431.1:c.497C>T | NP_001338360.1:p.Ala166Val | |
| NM_001351432.1:c.497C>T | NP_001338361.1:p.Ala166Val | |
| NM_001351433.1:c.497C>T | NP_001338362.1:p.Ala166Val | |
| XM_005252066.3:c.854C>T | XP_005252123.1:p.Ala285Val | |
| XM_005252067.4:c.854C>T | XP_005252124.1:p.Ala285Val | |
| XM_005252069.4:c.854C>T | XP_005252126.1:p.Ala285Val | |
| XM_006717150.3:c.767C>T | XP_006717213.1:p.Ala256Val | |
| XM_017014849.1:c.824C>T | XP_016870338.1:p.Ala275Val | |
| XR_001746328.2:n.1049C>T | ||
| XR_001746329.2:n.1001C>T | ||
| NM_001698.3:c.824C>T MANE Select | NP_001689.1:p.Ala275Val | |
| NM_001306190.2:c.737C>T | NP_001293119.1:p.Ala246Val | |
| NM_001351431.2:c.497C>T | NP_001338360.1:p.Ala166Val | |
| NM_001351432.2:c.497C>T | NP_001338361.1:p.Ala166Val | |
| NM_001351433.2:c.497C>T | NP_001338362.1:p.Ala166Val |