Linked Data
gnomAD v4:
11-118312740-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312740G>C , CM000673.2:g.118312740G>C | GRCh38 |
| NC_000011.9:g.118183455G>C , CM000673.1:g.118183455G>C | GRCh37 |
| NC_000011.8:g.117688665G>C | NCBI36 |
| NG_007383.1:g.13161G>C , LRG_38:g.13161G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.226G>C MANE Select | ENSP00000354566.4:p.Gly76Arg | |
| ENST00000361763.8:c.226G>C | ENSP00000354566.4:p.Gly76Arg | |
| ENST00000526146.5:n.772G>C | ||
| ENST00000528435.5:n.779G>C | ||
| ENST00000528600.1:c.208G>C | ENSP00000433975.1:p.Gly70Arg | |
| ENST00000529713.5:n.332G>C | ||
| ENST00000531913.1:n.597G>C | ||
| NM_000733.3:c.226G>C , LRG_38t1:c.226G>C | NP_000724.1:p.Gly76Arg | |
| NM_000733.4:c.226G>C MANE Select | NP_000724.1:p.Gly76Arg |