Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75579424G>T , CM000676.2:g.75579424G>T | GRCh38 |
| NC_000014.8:g.76045767G>T , CM000676.1:g.76045767G>T | GRCh37 |
| NC_000014.7:g.75115520G>T | NCBI36 |
| NG_027694.1:g.5828G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000238667.9:c.452G>T (FLVCR2) MANE Select | ENSP00000238667.4:p.Arg151Leu | |
| ENST00000238667.8:c.452G>T (FLVCR2) | ENSP00000238667.4:p.Arg151Leu | |
| NM_017791.2:c.452G>T (FLVCR2) | NP_060261.2:p.Arg151Leu | |
| NR_110552.1:n.165C>A (FLVCR2-AS1) | ||
| NM_017791.3:c.452G>T (FLVCR2) MANE Select | NP_060261.2:p.Arg151Leu |