Linked Data
ClinVar Variation Id:
2697102
ClinVar RCV Id:
RCV003582190
gnomAD v4:
1-53210613-G-A
MyVariant Identifiers:
chr1:g.53676285G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.53210613G>A , CM000663.2:g.53210613G>A | GRCh38 |
| NC_000001.10:g.53676285G>A , CM000663.1:g.53676285G>A | GRCh37 |
| NC_000001.9:g.53448873G>A | NCBI36 |
| NG_008035.1:g.19185G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371486.4:c.939G>A MANE Select | ENSP00000360541.3:p.Glu313= | |
| ENST00000635862.1:c.939G>A | ENSP00000490867.1:p.Glu313= | |
| ENST00000635888.1:c.*925G>A | ENSP00000490042.1:n.*925G>A | |
| ENST00000636239.1:c.*586G>A | ENSP00000490066.1:n.*586G>A | |
| ENST00000636867.1:c.939G>A | ENSP00000489631.1:p.Glu313= | |
| ENST00000636891.1:c.939G>A | ENSP00000490399.1:p.Glu313= | |
| ENST00000636935.1:c.341-2651G>A | ENSP00000489757.1:n.341-2651G>A | |
| ENST00000637252.1:c.939G>A | ENSP00000490492.1:p.Glu313= | |
| ENST00000637726.1:n.3139G>A | ||
| ENST00000638135.1:c.*586G>A | ENSP00000489756.1:n.*586G>A | |
| ENST00000371486.3:c.939G>A | ENSP00000360541.3:p.Glu313= | |
| NM_000098.2:c.939G>A | NP_000089.1:p.Glu313= | |
| XM_005270484.1:c.939G>A | XP_005270541.1:p.Glu313= | |
| NM_001330589.1:c.939G>A | NP_001317518.1:p.Glu313= | |
| NM_000098.3:c.939G>A MANE Select | NP_000089.1:p.Glu313= | |
| NM_001330589.2:c.939G>A | NP_001317518.1:p.Glu313= |