Linked Data
ClinVar Variation Id:
67333
ClinVar RCV Id:
RCV000058052
dbSNP Id:
rs199472969
gnomAD v4:
7-150951479-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150951479C>A , CM000669.2:g.150951479C>A | GRCh38 |
| NC_000007.13:g.150648567C>A , CM000669.1:g.150648567C>A | GRCh37 |
| NC_000007.12:g.150279500C>A | NCBI36 |
| NG_008916.1:g.31448G>T , LRG_288:g.31448G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000461280.2:n.1212G>T | ||
| ENST00000683359.1:n.38G>T | ||
| ENST00000684241.1:n.2747G>T | ||
| ENST00000262186.10:c.1914G>T MANE Select | ENSP00000262186.5:p.Lys638Asn | |
| ENST00000330883.9:c.894G>T | ENSP00000328531.4:p.Lys298Asn | |
| ENST00000262186.9:c.1914G>T | ENSP00000262186.5:p.Lys638Asn | |
| ENST00000330883.8:c.894G>T | ENSP00000328531.4:p.Lys298Asn | |
| ENST00000430723.4:c.1566G>T | ENSP00000387657.4:p.Lys522Asn | |
| ENST00000461280.1:n.1201G>T | ||
| ENST00000473610.5:n.1219G>T | ||
| ENST00000532957.5:n.2137G>T | ||
| NM_000238.3:c.1914G>T , LRG_288t1:c.1914G>T | NP_000229.1:p.Lys638Asn | |
| NM_001204798.1:c.894G>T | NP_001191727.1:p.Lys298Asn | |
| NM_172056.2:c.1914G>T , LRG_288t2:c.1914G>T | NP_742053.1:p.Lys638Asn | |
| NM_172057.2:c.894G>T , LRG_288t3:c.894G>T | NP_742054.1:p.Lys298Asn | |
| XM_011516185.1:c.1614G>T | XP_011514487.1:p.Lys538Asn | |
| XM_011516186.1:c.1914G>T | XP_011514488.1:p.Lys638Asn | |
| XM_011516185.2:c.1614G>T | XP_011514487.1:p.Lys538Asn | |
| XM_011516186.3:c.1914G>T | XP_011514488.1:p.Lys638Asn | |
| XM_017012195.1:c.1764G>T | XP_016867684.1:p.Lys588Asn | |
| XM_017012196.1:c.1737G>T | XP_016867685.1:p.Lys579Asn | |
| NM_000238.4:c.1914G>T MANE Select | NP_000229.1:p.Lys638Asn | |
| NM_001204798.2:c.894G>T | NP_001191727.1:p.Lys298Asn | |
| NM_172057.3:c.894G>T | NP_742054.1:p.Lys298Asn |