Linked Data
ClinVar Variation Id:
2734153
ClinVar RCV Id:
RCV003554925
dbSNP Id:
rs1659115204
gnomAD v4:
1-94418520-G-T
MyVariant Identifiers:
chr1:g.94884076G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94418520G>T , CM000663.2:g.94418520G>T | GRCh38 |
| NC_000001.10:g.94884076G>T , CM000663.1:g.94884076G>T | GRCh37 |
| NC_000001.9:g.94656664G>T | NCBI36 |
| NG_008865.1:g.5144G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370214.9:c.42G>T MANE Select | ENSP00000359233.4:p.Ser14= | |
| ENST00000647998.2:c.42G>T | ENSP00000497921.2:p.Ser14= | |
| ENST00000315713.5:c.42G>T | ENSP00000326880.5:p.Ser14= | |
| ENST00000370214.8:c.42G>T | ENSP00000359233.4:p.Ser14= | |
| NM_001122674.1:c.42G>T | NP_001116146.1:p.Ser14= | |
| NM_002858.3:c.42G>T | NP_002849.1:p.Ser14= | |
| XM_006710802.2:c.42G>T | XP_006710865.2:p.Ser14= | |
| NM_002858.4:c.42G>T MANE Select | NP_002849.1:p.Ser14= | |
| NM_001122674.2:c.42G>T | NP_001116146.1:p.Ser14= |