Linked Data
ClinVar Variation Id:
496502
dbSNP Id:
rs370212314
gnomAD v4:
17-58695120-G-T
PubMed:
PMID:26261251
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58695120G>T , CM000679.2:g.58695120G>T | GRCh38 |
| NC_000017.10:g.56772481G>T , CM000679.1:g.56772481G>T | GRCh37 |
| NC_000017.9:g.54127480G>T | NCBI36 |
| NG_023199.1:g.7519G>T , LRG_314:g.7519G>T | |
| NG_047169.1:g.1960C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461271.6:c.-17G>T | ENSP00000464056.2:n.-17G>T | |
| ENST00000697675.1:n.1429G>T | ||
| ENST00000697676.1:n.395G>T | ||
| ENST00000697677.1:n.1416G>T | ||
| ENST00000697678.1:n.237G>T | ||
| ENST00000697679.1:n.1409G>T | ||
| ENST00000697680.1:c.*1199G>T | ENSP00000513392.1:n.*1199G>T | |
| ENST00000697681.1:c.*1199G>T | ENSP00000513393.1:n.*1199G>T | |
| ENST00000697683.1:c.*1199G>T | ENSP00000513395.1:n.*1199G>T | |
| ENST00000697684.1:n.395G>T | ||
| ENST00000697685.1:c.*1199G>T | ENSP00000513396.1:n.*1199G>T | |
| ENST00000697686.1:c.-17G>T | ENSP00000513397.1:n.-17G>T | |
| ENST00000697687.1:n.381G>T | ||
| ENST00000697688.1:n.381G>T | ||
| ENST00000697689.1:c.*1038G>T | ENSP00000513398.1:n.*1038G>T | |
| ENST00000697690.1:c.335G>T | ENSP00000513399.1:p.Gly112Val | |
| ENST00000697691.1:c.*307G>T | ENSP00000513400.1:n.*307G>T | |
| ENST00000697692.1:c.*347G>T | ENSP00000513401.1:n.*347G>T | |
| ENST00000697693.1:n.1110G>T | ||
| ENST00000697694.1:c.-17G>T | ENSP00000513402.1:n.-17G>T | |
| ENST00000697695.1:n.942G>T | ||
| ENST00000337432.9:c.335G>T MANE Select | ENSP00000336701.4:p.Gly112Val | |
| ENST00000337432.8:c.335G>T | ENSP00000336701.4:p.Gly112Val | |
| ENST00000421782.3:c.335G>T | ENSP00000391450.2:p.Gly112Val | |
| ENST00000425173.5:c.131G>T | ENSP00000407282.1:p.Gly44Val | |
| ENST00000461271.5:c.-17G>T | ENSP00000464056.1:n.-17G>T | |
| ENST00000475762.5:c.*1038G>T | ENSP00000432421.1:n.*1038G>T | |
| ENST00000482007.5:c.335G>T | ENSP00000433332.1:p.Gly112Val | |
| ENST00000486827.1:c.*1199G>T | ENSP00000436761.1:n.*1199G>T | |
| ENST00000487525.5:c.335G>T | ENSP00000431637.1:p.Gly112Val | |
| ENST00000487921.5:n.247G>T | ||
| ENST00000583539.5:c.335G>T | ENSP00000463121.1:p.Gly112Val | |
| ENST00000584617.5:c.127-1573G>T | ||
| ENST00000622327.4:c.71G>T | ENSP00000482326.1:p.Gly24Val | |
| NM_002876.3:c.335G>T | NP_002867.1:p.Gly112Val | |
| NM_058216.2:c.335G>T | NP_478123.1:p.Gly112Val | |
| NR_103872.1:n.406G>T | ||
| NR_103873.1:n.303G>T | ||
| XM_006722001.2:c.335G>T | XP_006722064.1:p.Gly112Val | |
| XM_006722002.2:c.335G>T | XP_006722065.1:p.Gly112Val | |
| XM_006722004.2:c.-17G>T | XP_006722067.1:n.-17G>T | |
| XM_006722005.2:c.-17G>T | XP_006722068.1:n.-17G>T | |
| XM_011525092.1:c.-17G>T | XP_011523394.1:n.-17G>T | |
| XM_011525093.1:c.-17G>T | XP_011523395.1:n.-17G>T | |
| XM_011525094.1:c.-17G>T | XP_011523396.1:n.-17G>T | |
| XR_934513.1:n.408G>T | ||
| XR_934514.1:n.408G>T | ||
| XM_006722001.4:c.335G>T | XP_006722064.1:p.Gly112Val | |
| XM_006722002.4:c.335G>T | XP_006722065.1:p.Gly112Val | |
| XM_006722004.3:c.-17G>T | XP_006722067.1:n.-17G>T | |
| XM_006722005.3:c.-17G>T | XP_006722068.1:n.-17G>T | |
| XM_011525092.2:c.-17G>T | XP_011523394.1:n.-17G>T | |
| XM_011525093.2:c.-17G>T | XP_011523395.1:n.-17G>T | |
| XM_011525094.2:c.-17G>T | XP_011523396.1:n.-17G>T | |
| XM_017024914.1:c.-17G>T | XP_016880403.1:n.-17G>T | |
| XM_017024915.1:c.-17G>T | XP_016880404.1:n.-17G>T | |
| XM_017024916.1:c.-17G>T | XP_016880405.1:n.-17G>T | |
| XM_017024917.1:c.-17G>T | XP_016880406.1:n.-17G>T | |
| XM_017024918.2:c.-17G>T | XP_016880407.1:n.-17G>T | |
| XM_017024919.1:c.-17G>T | XP_016880408.1:n.-17G>T | |
| XR_934513.3:n.839G>T | ||
| XR_934514.3:n.839G>T | ||
| NM_058216.3:c.335G>T MANE Select | NP_478123.1:p.Gly112Val | |
| NR_103872.2:n.377G>T | ||
| NM_002876.4:c.335G>T | NP_002867.1:p.Gly112Val |