Linked Data
ClinVar Variation Id:
67503
ClinVar RCV Id:
RCV001841758
dbSNP Id:
rs199472863
gnomAD v2:
7-150656744-C-T
gnomAD v4:
7-150959656-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150959656C>T , CM000669.2:g.150959656C>T | GRCh38 |
| NC_000007.13:g.150656744C>T , CM000669.1:g.150656744C>T | GRCh37 |
| NC_000007.12:g.150287677C>T | NCBI36 |
| NG_008916.1:g.23271G>A , LRG_288:g.23271G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000684241.1:n.1221G>A | ||
| ENST00000262186.10:c.388G>A MANE Select | ENSP00000262186.5:p.Glu130Lys | |
| ENST00000262186.9:c.388G>A | ENSP00000262186.5:p.Glu130Lys | |
| ENST00000430723.4:c.211G>A | ENSP00000387657.4:p.Glu71Lys | |
| ENST00000532957.5:n.611G>A | ||
| NM_000238.3:c.388G>A , LRG_288t1:c.388G>A | NP_000229.1:p.Glu130Lys | |
| NM_172056.2:c.388G>A , LRG_288t2:c.388G>A | NP_742053.1:p.Glu130Lys | |
| XM_011516185.1:c.88G>A | XP_011514487.1:p.Glu30Lys | |
| XM_011516186.1:c.388G>A | XP_011514488.1:p.Glu130Lys | |
| XM_011516185.2:c.88G>A | XP_011514487.1:p.Glu30Lys | |
| XM_011516186.3:c.388G>A | XP_011514488.1:p.Glu130Lys | |
| XM_017012195.1:c.238G>A | XP_016867684.1:p.Glu80Lys | |
| XM_017012196.1:c.211G>A | XP_016867685.1:p.Glu71Lys | |
| NM_000238.4:c.388G>A MANE Select | NP_000229.1:p.Glu130Lys |