HGVS | Genome Assembly |
---|---|
NC_000011.10:g.113475356C>A , CM000673.2:g.113475356C>A | GRCh38 |
NC_000011.9:g.113346078C>A , CM000673.1:g.113346078C>A | GRCh37 |
NC_000011.8:g.112851288C>A | NCBI36 |
NG_008841.1:g.4924G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000362072.8:c.-312G>T MANE Select | ENSP00000354859.3:n.-312G>T | |
ENST00000362072.7:c.-312G>T | ENSP00000354859.3:n.-312G>T | |
ENST00000540600.5:n.34+302G>T | ||
NM_000795.4:c.-312G>T MANE Select | NP_000786.1:n.-312G>T | |
NM_016574.4:c.-312G>T | NP_057658.2:n.-312G>T |