Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117837137C>G , CM000670.2:g.117837137C>G | GRCh38 |
| NC_000008.10:g.118849376C>G , CM000670.1:g.118849376C>G | GRCh37 |
| NC_000008.9:g.118918557C>G | NCBI36 |
| NG_007455.2:g.279683G>C , LRG_493:g.279683G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000127.3:c.1027G>C MANE Select | NP_000118.2:p.Gly343Arg |
| ENST00000378204.7:c.1027G>C MANE Select | ENSP00000367446.3:p.Gly343Arg |
| NM_000127.2:c.1027G>C , LRG_493t1:c.1027G>C | NP_000118.2:p.Gly343Arg |
| ENST00000378204.6:c.1027G>C | ENSP00000367446.2:p.Gly343Arg |
| ENST00000436216.1:c.395G>C | |
| ENST00000436216.2:c.395G>C | |
| ENST00000437196.1:c.74-1586G>C | ENSP00000407299.1:n.74-1586G>C |
| ENST00000684189.1:n.494G>C |