HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20579803C>T , CM000686.2:g.20579803C>T | GRCh38 |
NC_000024.9:g.22741689C>T , CM000686.1:g.22741689C>T | GRCh37 |
NC_000024.8:g.21151077C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361365.7:c.100+112C>T MANE Select | ENSP00000354722.2:n.100+112C>T | |
ENST00000361365.6:c.100+112C>T | ENSP00000354722.2:n.100+112C>T | |
ENST00000382772.3:c.100+112C>T | ENSP00000372222.3:n.100+112C>T | |
ENST00000465253.1:n.194+112C>T | ||
NM_001278612.1:c.100+112C>T | NP_001265541.1:n.100+112C>T | |
NM_004681.3:c.100+112C>T | NP_004672.2:n.100+112C>T | |
NM_004681.4:c.100+112C>T MANE Select | NP_004672.2:n.100+112C>T | |
NM_001278612.2:c.100+112C>T | NP_001265541.1:n.100+112C>T |