Linked Data
ClinVar Variation Id:
264258
dbSNP Id:
rs794728035
gnomAD v2:
2-189849527-G-A
gnomAD v4:
2-188984801-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.188984801G>A , CM000664.2:g.188984801G>A | GRCh38 |
| NC_000002.11:g.189849527G>A , CM000664.1:g.189849527G>A | GRCh37 |
| NC_000002.10:g.189557772G>A | NCBI36 |
| NG_007404.1:g.15429G>A , LRG_3:g.15429G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450867.2:c.121G>A | ENSP00000415346.2:p.Asp41Asn | |
| ENST00000304636.9:c.121G>A MANE Select | ENSP00000304408.4:p.Asp41Asn | |
| ENST00000304636.7:c.121G>A | ENSP00000304408.3:p.Asp41Asn | |
| ENST00000317840.9:c.121G>A | ENSP00000315243.6:p.Asp41Asn | |
| ENST00000470167.1:n.217G>A | ||
| NM_000090.3:c.121G>A , LRG_3t1:c.121G>A | NP_000081.1:p.Asp41Asn | |
| NM_000090.4:c.121G>A MANE Select | NP_000081.2:p.Asp41Asn |