Linked Data
gnomAD v4:
2-27085297-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.27085297G>C , CM000664.2:g.27085297G>C | GRCh38 |
| NC_000002.11:g.27308165G>C , CM000664.1:g.27308165G>C | GRCh37 |
| NC_000002.10:g.27161669G>C | NCBI36 |
| NG_012199.1:g.3555G>C | |
| NG_046849.1:g.11731G>C | |
| NG_012199.2:g.3555G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380320.9:c.2713G>C MANE Select | ENSP00000369677.4:p.Gly905Arg | |
| ENST00000380320.8:c.2713G>C | ENSP00000369677.4:p.Gly905Arg | |
| ENST00000433140.1:c.705G>C | ||
| NM_007046.3:c.2713G>C | NP_008977.1:p.Gly905Arg | |
| XM_006711928.2:c.2575+289G>C | XP_006711991.1:n.2575+289G>C | |
| NM_007046.4:c.2713G>C MANE Select | NP_008977.1:p.Gly905Arg |