Linked Data
ClinVar Variation Id:
67527
dbSNP Id:
rs199472876
ExAC:
7:150655288 C / T
gnomAD v2:
7-150655288-C-T
gnomAD v3:
7-150958200-C-T
gnomAD v4:
7-150958200-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150958200C>T , CM000669.2:g.150958200C>T | GRCh38 |
| NC_000007.13:g.150655288C>T , CM000669.1:g.150655288C>T | GRCh37 |
| NC_000007.12:g.150286221C>T | NCBI36 |
| NG_008916.1:g.24727G>A , LRG_288:g.24727G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000684241.1:n.1608G>A | ||
| ENST00000262186.10:c.775G>A MANE Select | ENSP00000262186.5:p.Asp259Asn | |
| ENST00000262186.9:c.775G>A | ENSP00000262186.5:p.Asp259Asn | |
| ENST00000430723.4:c.427G>A | ENSP00000387657.4:p.Asp143Asn | |
| ENST00000532957.5:n.998G>A | ||
| NM_000238.3:c.775G>A , LRG_288t1:c.775G>A | NP_000229.1:p.Asp259Asn | |
| NM_172056.2:c.775G>A , LRG_288t2:c.775G>A | NP_742053.1:p.Asp259Asn | |
| XM_011516185.1:c.475G>A | XP_011514487.1:p.Asp159Asn | |
| XM_011516186.1:c.775G>A | XP_011514488.1:p.Asp259Asn | |
| XM_011516185.2:c.475G>A | XP_011514487.1:p.Asp159Asn | |
| XM_011516186.3:c.775G>A | XP_011514488.1:p.Asp259Asn | |
| XM_017012195.1:c.625G>A | XP_016867684.1:p.Asp209Asn | |
| XM_017012196.1:c.598G>A | XP_016867685.1:p.Asp200Asn | |
| NM_000238.4:c.775G>A MANE Select | NP_000229.1:p.Asp259Asn |