Linked Data
ClinVar Variation Id:
742698
ClinVar RCV Id:
RCV001462198
dbSNP Id:
rs756650132
ExAC:
10:121432117 A / G
gnomAD v2:
10-121432117-A-G
gnomAD v4:
10-119672605-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119672605A>G , CM000672.2:g.119672605A>G | GRCh38 |
| NC_000010.10:g.121432117A>G , CM000672.1:g.121432117A>G | GRCh37 |
| NC_000010.9:g.121422107A>G | NCBI36 |
| NG_016125.1:g.26236A>G , LRG_742:g.26236A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.858A>G MANE Select | ENSP00000358081.4:p.Pro286= | |
| ENST00000369085.7:c.858A>G | ENSP00000358081.3:p.Pro286= | |
| ENST00000450186.1:c.684A>G | ENSP00000410036.1:p.Pro228= | |
| NM_004281.3:c.858A>G , LRG_742t1:c.858A>G | NP_004272.2:p.Pro286= | |
| XM_005270287.1:c.858A>G | XP_005270344.1:p.Pro286= | |
| XM_005270287.2:c.858A>G | XP_005270344.1:p.Pro286= | |
| NM_004281.4:c.858A>G MANE Select | NP_004272.2:p.Pro286= |