Linked Data
ClinVar Variation Id:
853116
ClinVar RCV Id:
RCV001057863
dbSNP Id:
rs2062427019
gnomAD v4:
X-48688396-G-A
COSMIC:
COSM3424821
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48688396G>A , CM000685.2:g.48688396G>A | GRCh38 |
| NC_000023.10:g.48546785G>A , CM000685.1:g.48546785G>A | GRCh37 |
| NC_000023.9:g.48431729G>A | NCBI36 |
| NG_007877.1:g.9600G>A , LRG_125:g.9600G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474174.2:n.118G>A | ||
| ENST00000698625.1:c.874G>A | ENSP00000513844.1:p.Asp292Asn | |
| ENST00000698626.1:c.874G>A | ENSP00000513845.1:p.Asp292Asn | |
| ENST00000698635.1:c.874G>A | ENSP00000513850.1:p.Asp292Asn | |
| ENST00000376701.5:c.874G>A MANE Select | ENSP00000365891.4:p.Asp292Asn | |
| ENST00000376701.4:c.874G>A | ENSP00000365891.4:p.Asp292Asn | |
| ENST00000474174.1:n.118G>A | ||
| NM_000377.2:c.874G>A , LRG_125t1:c.874G>A | NP_000368.1:p.Asp292Asn | |
| XM_011543977.1:c.874G>A | XP_011542279.1:p.Asp292Asn | |
| XM_011543977.2:c.874G>A | XP_011542279.1:p.Asp292Asn | |
| XM_017029786.1:c.874G>A | XP_016885275.1:p.Asp292Asn | |
| NM_000377.3:c.874G>A MANE Select | NP_000368.1:p.Asp292Asn |