Linked Data
ClinVar Variation Id:
39105
ClinVar RCV Id:
RCV000032371
dbSNP Id:
rs199422296
gnomAD v4:
5-1279392-C-A
PubMed:
PMID:20301779
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1279392C>A , CM000667.2:g.1279392C>A | GRCh38 |
| NC_000005.9:g.1279507C>A , CM000667.1:g.1279507C>A | GRCh37 |
| NC_000005.8:g.1332507C>A | NCBI36 |
| NG_009265.1:g.20656G>T , LRG_343:g.20656G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000310581.10:c.2029G>T MANE Select | ENSP00000309572.5:p.Gly677Cys | |
| ENST00000656021.1:c.*1575G>T | ENSP00000499759.1:n.*1575G>T | |
| ENST00000310581.9:c.2029G>T | ENSP00000309572.5:p.Gly677Cys | |
| ENST00000334602.10:c.2029G>T | ENSP00000334346.6:p.Gly677Cys | |
| ENST00000460137.6:c.2029G>T | ENSP00000425003.1:p.Gly677Cys | |
| ENST00000484238.6:n.842G>T | ||
| ENST00000508104.2:c.2029G>T | ENSP00000426042.2:p.Gly677Cys | |
| NM_001193376.1:c.2029G>T | NP_001180305.1:p.Gly677Cys | |
| NM_198253.2:c.2029G>T , LRG_343t1:c.2029G>T | NP_937983.2:p.Gly677Cys | |
| XM_011514104.1:c.499G>T | XP_011512406.1:p.Gly167Cys | |
| XM_011514105.1:c.385G>T | XP_011512407.1:p.Gly129Cys | |
| XM_011514106.1:c.385G>T | XP_011512408.1:p.Gly129Cys | |
| NR_149162.1:n.2087G>T | ||
| NR_149163.1:n.2087G>T | ||
| NM_001193376.2:c.2029G>T | NP_001180305.1:p.Gly677Cys | |
| NM_198253.3:c.2029G>T MANE Select | NP_937983.2:p.Gly677Cys | |
| NR_149162.2:n.2108G>T | ||
| NR_149163.2:n.2108G>T | ||
| NM_001193376.3:c.2029G>T | NP_001180305.1:p.Gly677Cys | |
| NR_149162.3:n.2108G>T | ||
| NR_149163.3:n.2108G>T |