Linked Data
ClinVar Variation Id:
1611448
ClinVar RCV Id:
RCV002157847
dbSNP Id:
rs1178731855
gnomAD v2:
1-53675850-T-C
gnomAD v3:
1-53210178-T-C
gnomAD v4:
1-53210178-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.53210178T>C , CM000663.2:g.53210178T>C | GRCh38 |
| NC_000001.10:g.53675850T>C , CM000663.1:g.53675850T>C | GRCh37 |
| NC_000001.9:g.53448438T>C | NCBI36 |
| NG_008035.1:g.18750T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371486.4:c.504T>C MANE Select | ENSP00000360541.3:p.Ala168= | |
| ENST00000635862.1:c.504T>C | ENSP00000490867.1:p.Ala168= | |
| ENST00000635888.1:c.*490T>C | ENSP00000490042.1:n.*490T>C | |
| ENST00000636239.1:c.*151T>C | ENSP00000490066.1:n.*151T>C | |
| ENST00000636867.1:c.504T>C | ENSP00000489631.1:p.Ala168= | |
| ENST00000636891.1:c.504T>C | ENSP00000490399.1:p.Ala168= | |
| ENST00000636935.1:c.341-3086T>C | ENSP00000489757.1:n.341-3086T>C | |
| ENST00000637252.1:c.504T>C | ENSP00000490492.1:p.Ala168= | |
| ENST00000637726.1:n.2704T>C | ||
| ENST00000638135.1:c.*151T>C | ENSP00000489756.1:n.*151T>C | |
| ENST00000371486.3:c.504T>C | ENSP00000360541.3:p.Ala168= | |
| NM_000098.2:c.504T>C | NP_000089.1:p.Ala168= | |
| XM_005270484.1:c.504T>C | XP_005270541.1:p.Ala168= | |
| NM_001330589.1:c.504T>C | NP_001317518.1:p.Ala168= | |
| NM_000098.3:c.504T>C MANE Select | NP_000089.1:p.Ala168= | |
| NM_001330589.2:c.504T>C | NP_001317518.1:p.Ala168= |