HGVS | Genome Assembly |
---|---|
NC_000019.10:g.8679471C>A , CM000681.2:g.8679471C>A | GRCh38 |
NC_000019.9:g.8789735C>A , CM000681.1:g.8789735C>A | GRCh37 |
NC_000019.8:g.8650735C>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000570582.4:c.*1836C>A | ENSP00000500121.1:n.*1836C>A | |
ENST00000671902.2:c.*1836C>A | ENSP00000500604.1:n.*1836C>A | |
ENST00000673603.2:c.*1836C>A | ENSP00000499970.1:n.*1836C>A | |
ENST00000691075.1:c.*1836C>A MANE Select | ENSP00000509575.1:n.*1836C>A | |
NM_001378599.1:c.*1836C>A | NP_001365528.1:n.*1836C>A | |
NM_001378600.1:c.*1836C>A MANE Select | NP_001365529.1:n.*1836C>A | |
NM_001378601.1:c.*1836C>A | NP_001365530.1:n.*1836C>A |