Linked Data
gnomAD v4:
11-116832786-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116832786A>C , CM000673.2:g.116832786A>C | GRCh38 |
| NC_000011.9:g.116703502A>C , CM000673.1:g.116703502A>C | GRCh37 |
| NC_000011.8:g.116208712A>C | NCBI36 |
| NG_008949.1:g.7879A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227667.8:c.202A>C MANE Select | ENSP00000227667.2:p.Ser68Arg | |
| ENST00000227667.7:c.202A>C | ENSP00000227667.2:p.Ser68Arg | |
| ENST00000375345.3:c.256A>C | ENSP00000364494.1:p.Ser86Arg | |
| ENST00000630701.1:c.256A>C | ENSP00000486182.1:p.Ser86Arg | |
| NM_000040.1:c.202A>C | NP_000031.1:p.Ser68Arg | |
| NM_000040.2:c.202A>C | NP_000031.1:p.Ser68Arg | |
| NM_000040.3:c.202A>C MANE Select | NP_000031.1:p.Ser68Arg |