Linked Data
ClinVar Variation Id:
666425
dbSNP Id:
rs758031424
ExAC:
19:4099307 C / T
gnomAD v2:
19-4099307-C-T
gnomAD v3:
19-4099309-C-T
gnomAD v4:
19-4099309-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4099309C>T , CM000681.2:g.4099309C>T | GRCh38 |
| NC_000019.9:g.4099307C>T , CM000681.1:g.4099307C>T | GRCh37 |
| NC_000019.8:g.4050307C>T | NCBI36 |
| NG_007996.1:g.29820G>A , LRG_750:g.29820G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394867.9:n.1250G>A | ||
| ENST00000687128.1:n.1250G>A | ||
| ENST00000688002.1:n.1105G>A | ||
| ENST00000689792.1:n.715G>A | ||
| ENST00000262948.10:c.811G>A MANE Select | ENSP00000262948.4:p.Asp271Asn | |
| ENST00000262948.9:c.811G>A | ENSP00000262948.3:p.Asp271Asn | |
| ENST00000394867.8:c.520G>A | ENSP00000378336.1:p.Asp174Asn | |
| ENST00000593364.5:n.758G>A | ||
| ENST00000595715.1:n.626G>A | ||
| ENST00000597263.5:n.169+1710G>A | ||
| ENST00000599021.1:c.29+1710G>A | ||
| ENST00000600584.5:n.1371G>A | ||
| ENST00000601786.5:n.1112G>A | ||
| NM_030662.3:c.811G>A , LRG_750t1:c.811G>A | NP_109587.1:p.Asp271Asn | |
| XM_006722799.2:c.705+1710G>A | XP_006722862.1:n.705+1710G>A | |
| XM_011528133.1:c.241G>A | XP_011526435.1:p.Asp81Asn | |
| XM_017026989.1:c.811G>A | XP_016882478.1:p.Asp271Asn | |
| XM_017026990.1:c.705+1710G>A | XP_016882479.1:n.705+1710G>A | |
| NM_030662.4:c.811G>A MANE Select | NP_109587.1:p.Asp271Asn |