Linked Data
ClinVar Variation Id:
221004
dbSNP Id:
rs145619075
ExAC:
10:28224092 C / A
gnomAD v2:
10-28224092-C-A
gnomAD v3:
10-27935163-C-A
gnomAD v4:
10-27935163-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.27935163C>A , CM000672.2:g.27935163C>A | GRCh38 |
| NC_000010.10:g.28224092C>A , CM000672.1:g.28224092C>A | GRCh37 |
| NC_000010.9:g.28264098C>A | NCBI36 |
| NG_042820.1:g.68888G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305242.10:c.2342G>T MANE Select | ENSP00000306410.5:p.Gly781Val | |
| ENST00000672841.1:c.1418G>T | ENSP00000499983.1:p.Gly473Val | |
| ENST00000672877.1:c.917G>T | ENSP00000500120.1:p.Gly306Val | |
| ENST00000673384.1:c.1418G>T | ENSP00000500856.1:p.Gly473Val | |
| ENST00000673439.1:c.2342G>T | ENSP00000500782.1:p.Gly781Val | |
| ENST00000305242.9:c.2342G>T | ENSP00000306410.5:p.Gly781Val | |
| NM_001290020.1:c.2342G>T | NP_001276949.1:p.Gly781Val | |
| NM_001290021.1:c.917G>T | NP_001276950.1:p.Gly306Val | |
| NM_001312689.1:c.1418G>T | NP_001299618.1:p.Gly473Val | |
| NM_018076.3:c.2342G>T | NP_060546.2:p.Gly781Val | |
| NM_018076.4:c.2342G>T | NP_060546.2:p.Gly781Val | |
| XM_011519526.1:c.2342G>T | XP_011517828.1:p.Gly781Val | |
| XM_011519527.1:c.2342G>T | XP_011517829.1:p.Gly781Val | |
| XM_011519528.1:c.2342G>T | XP_011517830.1:p.Gly781Val | |
| XM_011519529.1:c.2342G>T | XP_011517831.1:p.Gly781Val | |
| XM_011519530.1:c.2342G>T | XP_011517832.1:p.Gly781Val | |
| XM_011519531.1:c.2342G>T | XP_011517833.1:p.Gly781Val | |
| XM_011519532.1:c.2132G>T | XP_011517834.1:p.Gly711Val | |
| XM_011519533.1:c.1418G>T | XP_011517835.1:p.Gly473Val | |
| XM_011519534.1:c.1418G>T | XP_011517836.1:p.Gly473Val | |
| XM_011519535.1:c.1256G>T | XP_011517837.1:p.Gly419Val | |
| XM_011519537.1:c.917G>T | XP_011517839.1:p.Gly306Val | |
| XM_024448049.1:c.2342G>T | XP_024303817.1:p.Gly781Val | |
| XM_024448050.1:c.2342G>T | XP_024303818.1:p.Gly781Val | |
| XM_024448051.1:c.2342G>T | XP_024303819.1:p.Gly781Val | |
| XM_024448052.1:c.2342G>T | XP_024303820.1:p.Gly781Val | |
| XM_024448053.1:c.2342G>T | XP_024303821.1:p.Gly781Val | |
| XM_024448054.1:c.2132G>T | XP_024303822.1:p.Gly711Val | |
| XM_024448055.1:c.1418G>T | XP_024303823.1:p.Gly473Val | |
| XM_024448056.1:c.1418G>T | XP_024303824.1:p.Gly473Val | |
| XM_024448057.1:c.1256G>T | XP_024303825.1:p.Gly419Val | |
| XM_024448058.1:c.917G>T | XP_024303826.1:p.Gly306Val | |
| NM_001290020.2:c.2342G>T | NP_001276949.1:p.Gly781Val | |
| NM_001290021.2:c.917G>T | NP_001276950.1:p.Gly306Val | |
| NM_001312689.2:c.1418G>T | NP_001299618.1:p.Gly473Val | |
| NM_018076.5:c.2342G>T MANE Select | NP_060546.2:p.Gly781Val |