HGVS | Genome Assembly |
---|---|
NC_000002.12:g.201623512C>T , CM000664.2:g.201623512C>T | GRCh38 |
NC_000002.11:g.202488235C>T , CM000664.1:g.202488235C>T | GRCh37 |
NC_000002.10:g.202196480C>T | NCBI36 |
NG_032049.1:g.25018G>A | |
NG_051007.1:g.671G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000621467.5:c.*743G>A | ENSP00000480508.2:n.*743G>A | |
ENST00000686475.1:n.1910G>A | ||
ENST00000409883.7:c.*743G>A MANE Select | ENSP00000386264.2:n.*743G>A | |
ENST00000409444.6:c.*743G>A | ENSP00000387203.2:n.*743G>A | |
ENST00000409883.6:c.*743G>A | ENSP00000386264.2:n.*743G>A | |
ENST00000495329.1:n.1109G>A | ||
NM_001044385.2:c.*743G>A | NP_001037850.1:n.*743G>A | |
NM_152388.3:c.*743G>A | NP_689601.2:n.*743G>A | |
NM_001044385.3:c.*743G>A MANE Select | NP_001037850.1:n.*743G>A | |
NM_152388.4:c.*743G>A | NP_689601.2:n.*743G>A |