Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.75579445C= , CM000676.2:g.75579445C= | GRCh38 |
| NC_000014.8:g.76045788C= , CM000676.1:g.76045788C= | GRCh37 |
| NC_000014.7:g.75115541C= | NCBI36 |
| NG_027694.1:g.5849C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_017791.3:c.473C= (FLVCR2) MANE Select | NP_060261.2:p.Ser158= |
| ENST00000238667.9:c.473C= (FLVCR2) MANE Select | ENSP00000238667.4:p.Ser158= |
| NM_017791.2:c.473C= (FLVCR2) | NP_060261.2:p.Ser158= |
| NR_110552.1:n.144G= (FLVCR2-AS1) | |
| ENST00000238667.8:c.473C= (FLVCR2) | ENSP00000238667.4:p.Ser158= |