HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23420367G>A , CM000676.2:g.23420367G>A | GRCh38 |
NC_000014.8:g.23889576G>A , CM000676.1:g.23889576G>A | GRCh37 |
NC_000014.7:g.22959416G>A | NCBI36 |
NG_007884.1:g.20295C>T , LRG_384:g.20295C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3337-133C>T MANE Select | ENSP00000347507.3:n.3337-133C>T | |
ENST00000355349.3:c.3337-133C>T | ENSP00000347507.3:n.3337-133C>T | |
NM_000257.3:c.3337-133C>T | NP_000248.2:n.3337-133C>T | |
XR_245686.3:n.3445-133C>T | ||
XM_017021340.1:c.3337-133C>T | XP_016876829.1:n.3337-133C>T | |
NM_000257.4:c.3337-133C>T MANE Select | NP_000248.2:n.3337-133C>T |