Linked Data
ClinVar Variation Id:
264302
ClinVar RCV Id:
RCV000248861
dbSNP Id:
rs886039118
gnomAD v4:
15-73323016-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73323016C>T , CM000677.2:g.73323016C>T | GRCh38 |
| NC_000015.9:g.73615357C>T , CM000677.1:g.73615357C>T | GRCh37 |
| NC_000015.8:g.71402410C>T | NCBI36 |
| NG_009063.1:g.51249G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.3077G>A MANE Select | ENSP00000261917.3:p.Ser1026Asn | |
| ENST00000261917.3:c.3077G>A | ENSP00000261917.3:p.Ser1026Asn | |
| NM_005477.2:c.3077G>A | NP_005468.1:p.Ser1026Asn | |
| XM_011521148.1:c.1859G>A | XP_011519450.1:p.Ser620Asn | |
| XM_011521148.2:c.1859G>A | XP_011519450.1:p.Ser620Asn | |
| NM_005477.3:c.3077G>A MANE Select | NP_005468.1:p.Ser1026Asn |