Linked Data
ClinVar Variation Id:
193106
ClinVar RCV Id:
RCV000173144
RCV000271089
RCV000362141
RCV000328523
RCV001104360
RCV001513849
RCV002381565
RCV002505244
dbSNP Id:
rs713040
ExAC:
11:5248243 A / G
gnomAD v2:
11-5248243-A-G
gnomAD v3:
11-5227013-A-G
gnomAD v4:
11-5227013-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5227013A>G , CM000673.2:g.5227013A>G | GRCh38 |
| NC_000011.9:g.5248243A>G , CM000673.1:g.5248243A>G | GRCh37 |
| NC_000011.8:g.5204819A>G | NCBI36 |
| NG_000007.3:g.70603T>C | |
| NG_059281.1:g.5059T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.9T>C | ENSP00000494175.1:p.His3= | |
| ENST00000335295.4:c.9T>C MANE Select | ENSP00000333994.3:p.His3= | |
| ENST00000380315.2:c.9T>C | ENSP00000369671.2:p.His3= | |
| ENST00000485743.1:n.60T>C | ||
| ENST00000633227.1:c.9T>C | ENSP00000488004.1:p.His3= | |
| NM_000518.4:c.9T>C | NP_000509.1:p.His3= | |
| NM_000518.5:c.9T>C MANE Select | NP_000509.1:p.His3= |