Linked Data
gnomAD v4:
11-89178219-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.89178219G>C , CM000673.2:g.89178219G>C | GRCh38 |
| NC_000011.9:g.88911387G>C , CM000673.1:g.88911387G>C | GRCh37 |
| NC_000011.8:g.88551035G>C | NCBI36 |
| NG_008748.1:g.5348G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263321.6:c.266G>C MANE Select | ENSP00000263321.4:p.Cys89Ser | |
| ENST00000263321.5:c.266G>C | ENSP00000263321.4:p.Cys89Ser | |
| ENST00000526139.1:n.327G>C | ||
| NM_000372.4:c.266G>C | NP_000363.1:p.Cys89Ser | |
| XM_011542970.1:c.266G>C | XP_011541272.1:p.Cys89Ser | |
| XM_011542970.2:c.266G>C | XP_011541272.1:p.Cys89Ser | |
| XR_001748321.1:n.2718-64686C>G | ||
| XR_001748322.1:n.2733-64686C>G | ||
| NM_000372.5:c.266G>C MANE Select | NP_000363.1:p.Cys89Ser |