Linked Data
dbSNP Id:
rs1366941418
gnomAD v3:
10-87966813-T-C
gnomAD v4:
10-87966813-T-C
MyVariant Identifiers:
chr10:g.87966813T>C (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87966813T>C , CM000672.2:g.87966813T>C | GRCh38 |
| NC_000010.10:g.89726570T>C , CM000672.1:g.89726570T>C | GRCh37 |
| NC_000010.9:g.89716550T>C | NCBI36 |
| NG_007466.2:g.108375T>C , LRG_311:g.108375T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000700029.2:c.*1341T>C | ENSP00000514759.2:n.*1341T>C | |
| ENST00000710265.1:c.*1582T>C | ENSP00000518161.1:n.*1582T>C | |
| ENST00000688158.2:n.3288T>C | ||
| ENST00000688922.2:c.*2383T>C | ENSP00000508742.2:n.*2383T>C | |
| ENST00000700021.1:c.*1341T>C | ENSP00000514757.1:n.*1341T>C | |
| ENST00000700024.1:n.3945T>C | ||
| ENST00000706954.1:c.*1341T>C | ENSP00000516674.1:n.*1341T>C | |
| ENST00000706955.1:c.*2588T>C | ENSP00000516675.1:n.*2588T>C | |
| ENST00000688158.1:c.*2664T>C | ENSP00000509254.1:n.*2664T>C | |
| ENST00000688308.1:c.*1341T>C | ENSP00000508752.1:n.*1341T>C | |
| ENST00000688922.1:c.2474T>C | ||
| ENST00000693560.1:c.*1341T>C | ENSP00000509861.1:n.*1341T>C | |
| ENST00000371953.8:c.*1341T>C MANE Select | ENSP00000361021.3:n.*1341T>C | |
| ENST00000371953.7:c.*1341T>C | ENSP00000361021.3:n.*1341T>C | |
| NM_000314.5:c.*1341T>C | NP_000305.3:n.*1341T>C | |
| NM_000314.6:c.*1341T>C | NP_000305.3:n.*1341T>C | |
| NM_001304717.2:c.*1341T>C | NP_001291646.2:n.*1341T>C | |
| NM_001304718.1:c.*1341T>C | NP_001291647.1:n.*1341T>C | |
| XM_006717926.2:c.*1341T>C | XP_006717989.1:n.*1341T>C | |
| XM_011539982.1:c.*1341T>C | XP_011538284.1:n.*1341T>C | |
| XR_945791.1:n.3123T>C | ||
| NM_000314.7:c.*1341T>C | NP_000305.3:n.*1341T>C | |
| NM_001304717.5:c.*1341T>C | NP_001291646.4:n.*1341T>C | |
| NM_001304718.2:c.*1341T>C | NP_001291647.1:n.*1341T>C | |
| NM_000314.8:c.*1341T>C MANE Select | NP_000305.3:n.*1341T>C |