Linked Data
ClinVar Variation Id:
1077370
dbSNP Id:
rs867171992
gnomAD v3:
10-87960926-C-T
gnomAD v4:
10-87960926-C-T
MyVariant Identifiers:
chr10:g.89720683C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87960926C>T , CM000672.2:g.87960926C>T | GRCh38 |
| NC_000010.10:g.89720683C>T , CM000672.1:g.89720683C>T | GRCh37 |
| NC_000010.9:g.89710663C>T | NCBI36 |
| NG_007466.2:g.102488C>T , LRG_311:g.102488C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.927C>T | ENSP00000514759.2:p.Phe309= | |
| ENST00000710265.1:c.834C>T | ENSP00000518161.1:p.Phe278= | |
| ENST00000472832.3:c.834C>T | ENSP00000483066.2:p.Phe278= | |
| ENST00000688158.2:n.1569C>T | ||
| ENST00000688922.2:c.*664C>T | ENSP00000508742.2:n.*664C>T | |
| ENST00000700021.1:c.789C>T | ENSP00000514757.1:p.Phe263= | |
| ENST00000700022.1:c.*173C>T | ENSP00000514758.1:n.*173C>T | |
| ENST00000700023.1:n.1992C>T | ||
| ENST00000700024.1:n.2226C>T | ||
| ENST00000700025.1:n.1603C>T | ||
| ENST00000700026.1:n.471C>T | ||
| ENST00000700029.1:c.761C>T | ||
| ENST00000706954.1:c.834C>T | ENSP00000516674.1:p.Phe278= | |
| ENST00000706955.1:c.*869C>T | ENSP00000516675.1:n.*869C>T | |
| ENST00000686459.1:c.*420C>T | ENSP00000508909.1:n.*420C>T | |
| ENST00000688158.1:c.*945C>T | ENSP00000509254.1:n.*945C>T | |
| ENST00000688308.1:c.834C>T | ENSP00000508752.1:p.Phe278= | |
| ENST00000688922.1:c.755C>T | ||
| ENST00000693560.1:c.1353C>T | ENSP00000509861.1:p.Phe451= | |
| ENST00000371953.8:c.834C>T MANE Select | ENSP00000361021.3:p.Phe278= | |
| ENST00000371953.7:c.834C>T | ENSP00000361021.3:p.Phe278= | |
| ENST00000472832.2:c.261C>T | ENSP00000483066.1:p.Phe87= | |
| NM_000314.5:c.834C>T | NP_000305.3:p.Phe278= | |
| NM_000314.6:c.834C>T | NP_000305.3:p.Phe278= | |
| NM_001304717.2:c.1353C>T | NP_001291646.2:p.Phe451= | |
| NM_001304718.1:c.243C>T | NP_001291647.1:p.Phe81= | |
| XM_006717926.2:c.789C>T | XP_006717989.1:p.Phe263= | |
| XM_011539981.1:c.834C>T | XP_011538283.1:p.Phe278= | |
| XM_011539982.1:c.738C>T | XP_011538284.1:p.Phe246= | |
| XR_945791.1:n.1404C>T | ||
| NM_000314.7:c.834C>T | NP_000305.3:p.Phe278= | |
| NM_001304717.5:c.1353C>T | NP_001291646.4:p.Phe451= | |
| NM_001304718.2:c.243C>T | NP_001291647.1:p.Phe81= | |
| NM_000314.8:c.834C>T MANE Select | NP_000305.3:p.Phe278= |