Linked Data
ClinVar Variation Id:
203666
dbSNP Id:
rs148035648
ExAC:
1:53675699 A / G
gnomAD v2:
1-53675699-A-G
gnomAD v3:
1-53210027-A-G
gnomAD v4:
1-53210027-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.53210027A>G , CM000663.2:g.53210027A>G | GRCh38 |
| NC_000001.10:g.53675699A>G , CM000663.1:g.53675699A>G | GRCh37 |
| NC_000001.9:g.53448287A>G | NCBI36 |
| NG_008035.1:g.18599A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371486.4:c.353A>G MANE Select | ENSP00000360541.3:p.Asp118Gly | |
| ENST00000635862.1:c.353A>G | ENSP00000490867.1:p.Asp118Gly | |
| ENST00000635888.1:c.*339A>G | ENSP00000490042.1:n.*339A>G | |
| ENST00000636239.1:c.246A>G | ENSP00000490066.1:p.Ter82Trp | |
| ENST00000636867.1:c.353A>G | ENSP00000489631.1:p.Asp118Gly | |
| ENST00000636891.1:c.353A>G | ENSP00000490399.1:p.Asp118Gly | |
| ENST00000636935.1:c.341-3237A>G | ENSP00000489757.1:n.341-3237A>G | |
| ENST00000637252.1:c.353A>G | ENSP00000490492.1:p.Asp118Gly | |
| ENST00000637726.1:n.2553A>G | ||
| ENST00000638135.1:c.165A>G | ENSP00000489756.1:p.Ter55Trp | |
| ENST00000371486.3:c.353A>G | ENSP00000360541.3:p.Asp118Gly | |
| NM_000098.2:c.353A>G | NP_000089.1:p.Asp118Gly | |
| XM_005270484.1:c.353A>G | XP_005270541.1:p.Asp118Gly | |
| NM_001330589.1:c.353A>G | NP_001317518.1:p.Asp118Gly | |
| NM_000098.3:c.353A>G MANE Select | NP_000089.1:p.Asp118Gly | |
| NM_001330589.2:c.353A>G | NP_001317518.1:p.Asp118Gly |