Linked Data
ClinVar Variation Id:
99909
dbSNP Id:
rs62636262
ExAC:
1:197297911 T / G
gnomAD v2:
1-197297911-T-G
gnomAD v3:
1-197328781-T-G
gnomAD v4:
1-197328781-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197328781T>G , CM000663.2:g.197328781T>G | GRCh38 |
| NC_000001.10:g.197297911T>G , CM000663.1:g.197297911T>G | GRCh37 |
| NC_000001.9:g.195564534T>G | NCBI36 |
| NG_008483.1:g.65504T>G | |
| NG_008483.2:g.132320T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367400.8:c.430T>G MANE Select | ENSP00000356370.3:p.Phe144Val | |
| ENST00000638467.1:c.430T>G | ENSP00000491102.1:p.Phe144Val | |
| ENST00000367399.6:c.430T>G | ENSP00000356369.2:p.Phe144Val | |
| ENST00000367400.7:c.430T>G | ENSP00000356370.3:p.Phe144Val | |
| ENST00000475659.1:n.567T>G | ||
| ENST00000484075.5:c.430T>G | ENSP00000433932.1:p.Phe144Val | |
| ENST00000535699.5:c.223T>G | ENSP00000438786.1:p.Phe75Val | |
| ENST00000538660.5:c.430T>G | ENSP00000438091.1:p.Phe144Val | |
| NM_001193640.1:c.430T>G | NP_001180569.1:p.Phe144Val | |
| NM_001257965.1:c.223T>G | NP_001244894.1:p.Phe75Val | |
| NM_001257966.1:c.430T>G | NP_001244895.1:p.Phe144Val | |
| NM_201253.2:c.430T>G | NP_957705.1:p.Phe144Val | |
| NR_047563.1:n.639T>G | ||
| NR_047564.1:n.639T>G | ||
| XM_011509365.1:c.430T>G | XP_011507667.1:p.Phe144Val | |
| XM_011509366.1:c.430T>G | XP_011507668.1:p.Phe144Val | |
| XM_011509367.1:c.430T>G | XP_011507669.1:p.Phe144Val | |
| XM_011509368.1:c.71-15500T>G | XP_011507670.1:n.71-15500T>G | |
| XM_011509365.2:c.430T>G | XP_011507667.1:p.Phe144Val | |
| XM_017000851.1:c.-274T>G | XP_016856340.1:n.-274T>G | |
| XM_017000852.1:c.430T>G | XP_016856341.1:p.Phe144Val | |
| NM_201253.3:c.430T>G MANE Select | NP_957705.1:p.Phe144Val | |
| NM_001193640.2:c.430T>G | NP_001180569.1:p.Phe144Val | |
| NM_001257965.2:c.223T>G | NP_001244894.1:p.Phe75Val | |
| NR_047563.2:n.591T>G | ||
| NR_047564.2:n.591T>G | ||
| NM_001257966.2:c.430T>G | NP_001244895.1:p.Phe144Val |