HGVS | Genome Assembly |
---|---|
NC_000021.9:g.36140133C>T , CM000683.2:g.36140133C>T | GRCh38 |
NC_000021.8:g.37512431C>T , CM000683.1:g.37512431C>T | GRCh37 |
NC_000021.7:g.36434301C>T | NCBI36 |
NG_052818.1:g.10233C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000290354.6:c.397+2201C>T (CBR3) MANE Select | ENSP00000290354.5:n.397+2201C>T | |
ENST00000290354.5:c.397+2201C>T (CBR3) | ENSP00000290354.5:n.397+2201C>T | |
NM_001236.3:c.397+2201C>T (CBR3) | NP_001227.1:n.397+2201C>T | |
NR_038892.1:n.192+6123G>A (CBR3-AS1) | ||
NR_038893.1:n.192+6123G>A (CBR3-AS1) | ||
XM_011529772.1:c.398-1791C>T (CBR3) | XP_011528074.1:n.398-1791C>T | |
XM_011529772.2:c.398-1791C>T (CBR3) | XP_011528074.1:n.398-1791C>T | |
NM_001236.4:c.397+2201C>T (CBR3) MANE Select | NP_001227.1:n.397+2201C>T |