HGVS | Genome Assembly |
---|---|
NC_000014.9:g.74500141C>T , CM000676.2:g.74500141C>T | GRCh38 |
NC_000014.8:g.74966844C>T , CM000676.1:g.74966844C>T | GRCh37 |
NC_000014.7:g.74036597C>T | NCBI36 |
NG_021486.1:g.117191G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261978.9:c.*743G>A MANE Select | ENSP00000261978.4:n.*743G>A | |
ENST00000261978.8:c.*743G>A | ENSP00000261978.4:n.*743G>A | |
NM_000428.2:c.*743G>A | NP_000419.1:n.*743G>A | |
XM_011536765.1:c.*743G>A | XP_011535067.1:n.*743G>A | |
XM_011536766.1:c.*743G>A | XP_011535068.1:n.*743G>A | |
XM_011536767.1:c.*743G>A | XP_011535069.1:n.*743G>A | |
XM_011536765.2:c.*743G>A | XP_011535067.1:n.*743G>A | |
NM_000428.3:c.*743G>A MANE Select | NP_000419.1:n.*743G>A |