Linked Data
ClinVar Variation Id:
1463375
ClinVar RCV Id:
RCV001997689
dbSNP Id:
rs2134167600
MyVariant Identifiers:
chr10:g.69926052A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.68166295A>T , CM000672.2:g.68166295A>T | GRCh38 |
| NC_000010.10:g.69926052A>T , CM000672.1:g.69926052A>T | GRCh37 |
| NC_000010.9:g.69596058A>T | NCBI36 |
| NG_032118.1:g.65179A>T , LRG_410:g.65179A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354393.7:c.777A>T | ENSP00000346369.2:p.Gly259= | |
| ENST00000373675.4:c.1602A>T | ENSP00000362779.4:p.Gly534= | |
| ENST00000540630.6:c.1656A>T | ENSP00000441668.3:p.Gly552= | |
| ENST00000613327.5:c.1602A>T | ENSP00000480757.2:p.Gly534= | |
| ENST00000687572.1:c.480A>T | ENSP00000510427.1:p.Gly160= | |
| ENST00000687705.1:c.*1851A>T | ENSP00000509639.1:n.*1851A>T | |
| ENST00000688812.1:c.1578A>T | ENSP00000510658.1:p.Gly526= | |
| ENST00000689002.1:n.654A>T | ||
| ENST00000690544.1:c.*873A>T | ENSP00000508989.1:n.*873A>T | |
| ENST00000358913.10:c.1602A>T MANE Select | ENSP00000351790.5:p.Gly534= | |
| ENST00000354393.6:c.777A>T | ENSP00000346369.2:p.Gly259= | |
| ENST00000358913.9:c.1602A>T | ENSP00000351790.5:p.Gly534= | |
| ENST00000540630.5:c.1602A>T | ENSP00000441668.2:p.Gly534= | |
| ENST00000613327.4:c.720A>T | ENSP00000480757.1:p.Gly240= | |
| NM_001256267.1:c.1602A>T | NP_001243196.1:p.Gly534= | |
| NM_001256268.1:c.720A>T | NP_001243197.1:p.Gly240= | |
| NM_032578.3:c.1602A>T , LRG_410t1:c.1602A>T | NP_115967.2:p.Gly534= | |
| NR_045662.3:n.1029A>T | ||
| NR_045663.3:n.1870A>T | ||
| XM_006718043.2:c.1656A>T | XP_006718106.1:p.Gly552= | |
| XM_011540292.1:c.1632A>T | XP_011538594.1:p.Gly544= | |
| XM_017016833.1:c.1680A>T | XP_016872322.1:p.Gly560= | |
| XM_017016834.2:c.1602A>T | XP_016872323.1:p.Gly534= | |
| XM_024448236.1:c.480A>T | XP_024304004.1:p.Gly160= | |
| NR_045662.4:n.1139A>T | ||
| NR_045663.4:n.1815A>T | ||
| NM_001256267.2:c.1602A>T | NP_001243196.1:p.Gly534= | |
| NM_001256268.2:c.720A>T | NP_001243197.1:p.Gly240= | |
| NM_032578.4:c.1602A>T MANE Select | NP_115967.2:p.Gly534= |