Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94408815G>C , CM000669.2:g.94408815G>C | GRCh38 |
| NC_000007.13:g.94038127G>C , CM000669.1:g.94038127G>C | GRCh37 |
| NC_000007.12:g.93876063G>C | NCBI36 |
| NG_007405.1:g.19255G>C , LRG_2:g.19255G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297268.11:c.784G>C MANE Select | ENSP00000297268.6:p.Gly262Arg | |
| ENST00000297268.10:c.784G>C | ENSP00000297268.6:p.Gly262Arg | |
| ENST00000620463.1:c.778G>C | ENSP00000477719.1:p.Gly260Arg | |
| NM_000089.3:c.784G>C , LRG_2t1:c.784G>C | NP_000080.2:p.Gly262Arg | |
| NM_000089.4:c.784G>C MANE Select | NP_000080.2:p.Gly262Arg |