Linked Data
ClinVar Variation Id:
2073229
ClinVar RCV Id:
RCV002971722
dbSNP Id:
rs1190622666
gnomAD v2:
10-121429441-C-T
gnomAD v4:
10-119669929-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119669929C>T , CM000672.2:g.119669929C>T | GRCh38 |
| NC_000010.10:g.121429441C>T , CM000672.1:g.121429441C>T | GRCh37 |
| NC_000010.9:g.121419431C>T | NCBI36 |
| NG_016125.1:g.23560C>T , LRG_742:g.23560C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.259C>T MANE Select | ENSP00000358081.4:p.Pro87Ser | |
| ENST00000369085.7:c.259C>T | ENSP00000358081.3:p.Pro87Ser | |
| ENST00000450186.1:c.85C>T | ENSP00000410036.1:p.Pro29Ser | |
| NM_004281.3:c.259C>T , LRG_742t1:c.259C>T | NP_004272.2:p.Pro87Ser | |
| XM_005270287.1:c.259C>T | XP_005270344.1:p.Pro87Ser | |
| XM_005270287.2:c.259C>T | XP_005270344.1:p.Pro87Ser | |
| NM_004281.4:c.259C>T MANE Select | NP_004272.2:p.Pro87Ser |