Linked Data
gnomAD v4:
11-89284981-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.89284981T>C , CM000673.2:g.89284981T>C | GRCh38 |
| NC_000011.9:g.89018149T>C , CM000673.1:g.89018149T>C | GRCh37 |
| NC_000011.8:g.88657797T>C | NCBI36 |
| NG_008748.1:g.112110T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263321.6:c.1366+27T>C MANE Select | ENSP00000263321.4:n.1366+27T>C | |
| ENST00000263321.5:c.1366+27T>C | ENSP00000263321.4:n.1366+27T>C | |
| ENST00000528243.1:n.364+27T>C | ||
| NM_000372.4:c.1366+27T>C | NP_000363.1:n.1366+27T>C | |
| XM_011542970.1:c.1366+27T>C | XP_011541272.1:n.1366+27T>C | |
| XM_011542970.2:c.1366+27T>C | XP_011541272.1:n.1366+27T>C | |
| XR_001748321.1:n.2456+1053A>G | ||
| XR_001748322.1:n.2457+1053A>G | ||
| NM_000372.5:c.1366+27T>C MANE Select | NP_000363.1:n.1366+27T>C |