Linked Data
gnomAD v4:
11-118312635-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312635T>C , CM000673.2:g.118312635T>C | GRCh38 |
| NC_000011.9:g.118183350T>C , CM000673.1:g.118183350T>C | GRCh37 |
| NC_000011.8:g.117688560T>C | NCBI36 |
| NG_007383.1:g.13056T>C , LRG_38:g.13056T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.121T>C MANE Select | ENSP00000354566.4:p.Ser41Pro | |
| ENST00000361763.8:c.121T>C | ENSP00000354566.4:p.Ser41Pro | |
| ENST00000526146.5:n.667T>C | ||
| ENST00000528435.5:n.674T>C | ||
| ENST00000528600.1:c.103T>C | ENSP00000433975.1:p.Ser35Pro | |
| ENST00000529713.5:n.227T>C | ||
| ENST00000531913.1:n.492T>C | ||
| NM_000733.3:c.121T>C , LRG_38t1:c.121T>C | NP_000724.1:p.Ser41Pro | |
| NM_000733.4:c.121T>C MANE Select | NP_000724.1:p.Ser41Pro |