Linked Data
ClinVar Variation Id:
1158906
ClinVar RCV Id:
RCV001502494
dbSNP Id:
rs2132621456
gnomAD v4:
10-49524530-G-A
MyVariant Identifiers:
chr10:g.50732576G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.49524530G>A , CM000672.2:g.49524530G>A | GRCh38 |
| NC_000010.10:g.50732576G>A , CM000672.1:g.50732576G>A | GRCh37 |
| NC_000010.9:g.50402582G>A | NCBI36 |
| NG_009442.1:g.19572C>T , LRG_465:g.19572C>T | |
| NG_033155.1:g.4752C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355832.10:c.900C>T MANE Select | ENSP00000348089.5:p.Ala300= | |
| ENST00000447839.7:c.900C>T MANE Plus Clinical | ENSP00000387966.2:p.Ala300= | |
| ENST00000679596.1:c.*529C>T | ENSP00000504862.1:n.*529C>T | |
| ENST00000679811.1:n.983C>T | ||
| ENST00000680107.1:c.652+3887C>T | ENSP00000505909.1:n.652+3887C>T | |
| ENST00000680233.1:n.993C>T | ||
| ENST00000681632.1:n.978C>T | ||
| ENST00000681659.1:c.900C>T | ENSP00000505631.1:p.Ala300= | |
| ENST00000355832.9:c.900C>T | ENSP00000348089.5:p.Ala300= | |
| ENST00000447839.6:c.900C>T | ENSP00000387966.2:p.Ala300= | |
| ENST00000515869.1:c.900C>T | ENSP00000423550.1:p.Ala300= | |
| NM_000124.3:c.900C>T | NP_000115.1:p.Ala300= | |
| NM_001277058.1:c.900C>T | NP_001263987.1:p.Ala300= | |
| NM_001277059.1:c.900C>T | NP_001263988.1:p.Ala300= | |
| NM_001346440.1:c.900C>T | NP_001333369.1:p.Ala300= | |
| NM_000124.4:c.900C>T MANE Select | NP_000115.1:p.Ala300= | |
| NM_001277058.2:c.900C>T MANE Plus Clinical | NP_001263987.1:p.Ala300= | |
| NM_001277059.2:c.900C>T | NP_001263988.1:p.Ala300= | |
| NM_001346440.2:c.900C>T | NP_001333369.1:p.Ala300= |