Linked Data
ClinVar Variation Id:
1555091
ClinVar RCV Id:
RCV002199805
dbSNP Id:
rs2134063295
gnomAD v4:
10-119669955-C-T
MyVariant Identifiers:
chr10:g.121429467C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119669955C>T , CM000672.2:g.119669955C>T | GRCh38 |
| NC_000010.10:g.121429467C>T , CM000672.1:g.121429467C>T | GRCh37 |
| NC_000010.9:g.121419457C>T | NCBI36 |
| NG_016125.1:g.23586C>T , LRG_742:g.23586C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.285C>T MANE Select | ENSP00000358081.4:p.Pro95= | |
| ENST00000369085.7:c.285C>T | ENSP00000358081.3:p.Pro95= | |
| ENST00000450186.1:c.111C>T | ENSP00000410036.1:p.Pro37= | |
| NM_004281.3:c.285C>T , LRG_742t1:c.285C>T | NP_004272.2:p.Pro95= | |
| XM_005270287.1:c.285C>T | XP_005270344.1:p.Pro95= | |
| XM_005270287.2:c.285C>T | XP_005270344.1:p.Pro95= | |
| NM_004281.4:c.285C>T MANE Select | NP_004272.2:p.Pro95= |