Linked Data
ClinVar Variation Id:
820479
dbSNP Id:
rs921435798
gnomAD v3:
17-58692644-A-G
gnomAD v4:
17-58692644-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58692644A>G , CM000679.2:g.58692644A>G | GRCh38 |
| NC_000017.10:g.56770005A>G , CM000679.1:g.56770005A>G | GRCh37 |
| NC_000017.9:g.54125004A>G | NCBI36 |
| NG_023199.1:g.5043A>G , LRG_314:g.5043A>G | |
| NG_047169.1:g.4436T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000461271.6:c.-248A>G | ENSP00000464056.2:n.-248A>G | |
| ENST00000697675.1:n.72A>G | ||
| ENST00000697676.1:n.61A>G | ||
| ENST00000697677.1:n.59A>G | ||
| ENST00000697678.1:n.47+12A>G | ||
| ENST00000697679.1:n.52A>G | ||
| ENST00000697680.1:c.1A>G | ENSP00000513392.1:p.Met1Val | |
| ENST00000697681.1:c.1A>G | ENSP00000513393.1:p.Met1Val | |
| ENST00000697683.1:c.1A>G | ENSP00000513395.1:p.Met1Val | |
| ENST00000697684.1:n.61A>G | ||
| ENST00000697685.1:c.1A>G | ENSP00000513396.1:p.Met1Val | |
| ENST00000697686.1:c.-207+12A>G | ENSP00000513397.1:n.-207+12A>G | |
| ENST00000697687.1:n.47A>G | ||
| ENST00000697688.1:n.47A>G | ||
| ENST00000697689.1:c.1A>G | ENSP00000513398.1:p.Met1Val | |
| ENST00000697690.1:c.1A>G | ENSP00000513399.1:p.Met1Val | |
| ENST00000697691.1:c.1A>G | ENSP00000513400.1:p.Met1Val | |
| ENST00000697692.1:c.1A>G | ENSP00000513401.1:p.Met1Val | |
| ENST00000337432.9:c.1A>G MANE Select | ENSP00000336701.4:p.Met1Val | |
| ENST00000337432.8:c.1A>G | ENSP00000336701.4:p.Met1Val | |
| ENST00000421782.3:c.1A>G | ENSP00000391450.2:p.Met1Val | |
| ENST00000461271.5:c.-248A>G | ENSP00000464056.1:n.-248A>G | |
| ENST00000475762.5:c.1A>G | ENSP00000432421.1:p.Met1Val | |
| ENST00000476741.2:n.43A>G | ||
| ENST00000482007.5:c.1A>G | ENSP00000433332.1:p.Met1Val | |
| ENST00000486827.1:c.1A>G | ENSP00000436761.1:p.Met1Val | |
| ENST00000487525.5:c.1A>G | ENSP00000431637.1:p.Met1Val | |
| ENST00000487921.5:n.57+12A>G | ||
| ENST00000583539.5:c.1A>G | ENSP00000463121.1:p.Met1Val | |
| NM_002876.3:c.1A>G | NP_002867.1:p.Met1Val | |
| NM_058216.2:c.1A>G | NP_478123.1:p.Met1Val | |
| NR_103872.1:n.72A>G | ||
| NR_103873.1:n.72A>G | ||
| XM_006722001.2:c.1A>G | XP_006722064.1:p.Met1Val | |
| XM_006722002.2:c.1A>G | XP_006722065.1:p.Met1Val | |
| XM_006722004.2:c.-248A>G | XP_006722067.1:n.-248A>G | |
| XM_006722005.2:c.-207+12A>G | XP_006722068.1:n.-207+12A>G | |
| XM_011525092.1:c.-548A>G | XP_011523394.1:n.-548A>G | |
| XM_011525093.1:c.-709A>G | XP_011523395.1:n.-709A>G | |
| XR_934513.1:n.74A>G | ||
| XR_934514.1:n.74A>G | ||
| XM_006722001.4:c.1A>G | XP_006722064.1:p.Met1Val | |
| XM_006722002.4:c.1A>G | XP_006722065.1:p.Met1Val | |
| XM_006722004.3:c.-248A>G | XP_006722067.1:n.-248A>G | |
| XM_006722005.3:c.-207+12A>G | XP_006722068.1:n.-207+12A>G | |
| XM_017024914.1:c.-248A>G | XP_016880403.1:n.-248A>G | |
| XM_017024916.1:c.-548A>G | XP_016880405.1:n.-548A>G | |
| XM_017024917.1:c.-207+12A>G | XP_016880406.1:n.-207+12A>G | |
| XM_017024918.2:c.-522A>G | XP_016880407.1:n.-522A>G | |
| XR_934513.3:n.505A>G | ||
| XR_934514.3:n.505A>G | ||
| NM_058216.3:c.1A>G MANE Select | NP_478123.1:p.Met1Val | |
| NR_103872.2:n.43A>G | ||
| NM_002876.4:c.1A>G | NP_002867.1:p.Met1Val |