HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75578902C>T , CM000676.2:g.75578902C>T | GRCh38 |
NC_000014.8:g.76045245C>T , CM000676.1:g.76045245C>T | GRCh37 |
NC_000014.7:g.75114998C>T | NCBI36 |
NG_027694.1:g.5306C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000238667.9:c.-71C>T (FLVCR2) MANE Select | ENSP00000238667.4:n.-71C>T | |
ENST00000238667.8:c.-71C>T (FLVCR2) | ENSP00000238667.4:n.-71C>T | |
NM_017791.2:c.-71C>T (FLVCR2) | NP_060261.2:n.-71C>T | |
NR_110552.1:n.687G>A (FLVCR2-AS1) | ||
NM_017791.3:c.-71C>T (FLVCR2) MANE Select | NP_060261.2:n.-71C>T |