HGVS | Genome Assembly |
---|---|
NC_000021.9:g.36135370C>A , CM000683.2:g.36135370C>A | GRCh38 |
NC_000021.8:g.37507668C>A , CM000683.1:g.37507668C>A | GRCh37 |
NC_000021.7:g.36429538C>A | NCBI36 |
NG_052818.1:g.5470C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000290354.6:c.178C>A (CBR3) MANE Select | ENSP00000290354.5:p.His60Asn | |
ENST00000290354.5:c.178C>A (CBR3) | ENSP00000290354.5:p.His60Asn | |
NM_001236.3:c.178C>A (CBR3) | NP_001227.1:p.His60Asn | |
NR_038892.1:n.193-1609G>T (CBR3-AS1) | ||
NR_038893.1:n.193-2296G>T (CBR3-AS1) | ||
XM_011529772.1:c.178C>A (CBR3) | XP_011528074.1:p.His60Asn | |
XM_011529772.2:c.178C>A (CBR3) | XP_011528074.1:p.His60Asn | |
NM_001236.4:c.178C>A (CBR3) MANE Select | NP_001227.1:p.His60Asn |