Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23429037C>G , CM000676.2:g.23429037C>G | GRCh38 |
| NC_000014.8:g.23898246C>G , CM000676.1:g.23898246C>G | GRCh37 |
| NC_000014.7:g.22968086C>G | NCBI36 |
| NG_007884.1:g.11625G>C , LRG_384:g.11625G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000355349.4:c.1325G>C MANE Select | ENSP00000347507.3:p.Arg442Pro | |
| ENST00000355349.3:c.1325G>C | ENSP00000347507.3:p.Arg442Pro | |
| NM_000257.3:c.1325G>C | NP_000248.2:p.Arg442Pro | |
| XR_245686.3:n.1431G>C | ||
| XM_017021340.1:c.1325G>C | XP_016876829.1:p.Arg442Pro | |
| NM_000257.4:c.1325G>C MANE Select | NP_000248.2:p.Arg442Pro |