HGVS | Genome Assembly |
---|---|
NC_000014.9:g.91272549C>A , CM000676.2:g.91272549C>A | GRCh38 |
NC_000014.8:g.91738893C>A , CM000676.1:g.91738893C>A | GRCh37 |
NC_000014.7:g.90808646C>A | NCBI36 |
NG_033118.1:g.150296G>T | |
NG_033118.2:g.150296G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389857.11:c.*76G>T MANE Select | ENSP00000374507.6:n.*76G>T | |
ENST00000331194.8:c.*76G>T | ENSP00000330332.8:n.*76G>T | |
ENST00000389857.10:c.*76G>T | ENSP00000374507.6:n.*76G>T | |
ENST00000556726.5:c.2391G>T | ||
NM_001080414.3:c.*76G>T | NP_001073883.2:n.*76G>T | |
XM_011536796.1:c.*76G>T | XP_011535098.1:n.*76G>T | |
XM_011536796.2:c.*76G>T | XP_011535098.1:n.*76G>T | |
XM_017021336.1:c.*76G>T | XP_016876825.1:n.*76G>T | |
NM_001080414.4:c.*76G>T MANE Select | NP_001073883.2:n.*76G>T |