HGVS | Genome Assembly |
---|---|
NC_000001.11:g.161222402A>T , CM000663.2:g.161222402A>T | GRCh38 |
NC_000001.10:g.161192192A>T , CM000663.1:g.161192192A>T | GRCh37 |
NC_000001.9:g.159458816A>T | NCBI36 |
NG_012043.1:g.6227T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367990.7:c.*3T>A MANE Select | ENSP00000356969.3:n.*3T>A | |
ENST00000463812.1:c.*3T>A | ENSP00000476890.1:n.*3T>A | |
ENST00000464492.5:c.*3T>A | ENSP00000476911.1:n.*3T>A | |
ENST00000468465.5:c.*3T>A | ENSP00000476662.1:n.*3T>A | |
ENST00000470459.6:c.*3T>A | ENSP00000477031.1:n.*3T>A | |
ENST00000481413.1:n.817T>A | ||
ENST00000481511.5:c.*303T>A | ENSP00000477054.1:n.*303T>A | |
ENST00000491350.1:c.*89T>A | ENSP00000477353.1:n.*89T>A | |
NM_001643.1:c.*3T>A | NP_001634.1:n.*3T>A | |
NM_001643.2:c.*3T>A MANE Select | NP_001634.1:n.*3T>A |