Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.23380137G>C , CM000685.2:g.23380137G>C | GRCh38 |
| NC_000023.10:g.23398254G>C , CM000685.1:g.23398254G>C | GRCh37 |
| NC_000023.9:g.23308175G>C | NCBI36 |
| NG_021300.1:g.50270G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_173495.3:c.898G>C MANE Select | NP_775766.2:p.Gly300Arg |
| ENST00000379361.5:c.898G>C MANE Select | ENSP00000368666.4:p.Gly300Arg |
| NM_173495.2:c.898G>C | NP_775766.2:p.Gly300Arg |
| ENST00000379361.4:c.898G>C | ENSP00000368666.4:p.Gly300Arg |
| ENST00000456522.1:c.159-12394G>C | |
| ENST00000616022.1:c.583G>C | ENSP00000478663.1:p.Gly195Arg |
| XM_011545449.1:c.898G>C | XP_011543751.1:p.Gly300Arg |
| XM_011545449.3:c.898G>C | XP_011543751.1:p.Gly300Arg |