HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67740427G>T , CM000666.2:g.67740427G>T | GRCh38 |
NC_000004.11:g.68606145G>T , CM000666.1:g.68606145G>T | GRCh37 |
NC_000004.10:g.68288740G>T | NCBI36 |
NG_009293.1:g.20660C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.*53C>A MANE Select | ENSP00000226413.5:n.*53C>A | |
ENST00000226413.4:c.*53C>A | ENSP00000226413.4:n.*53C>A | |
NM_000406.2:c.*53C>A | NP_000397.1:n.*53C>A | |
NM_001012763.1:c.*162C>A | NP_001012781.1:n.*162C>A | |
NM_000406.3:c.*53C>A MANE Select | NP_000397.1:n.*53C>A | |
NM_001012763.2:c.*162C>A | NP_001012781.1:n.*162C>A |