HGVS | Genome Assembly |
---|---|
NC_000008.11:g.23682904C>T , CM000670.2:g.23682904C>T | GRCh38 |
NC_000008.10:g.23540417C>T , CM000670.1:g.23540417C>T | GRCh37 |
NC_000008.9:g.23596362C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000380871.5:c.-15G>A MANE Select | ENSP00000370253.4:n.-15G>A | |
ENST00000380871.4:c.-15G>A | ENSP00000370253.4:n.-15G>A | |
NM_006167.3:c.-15G>A | NP_006158.2:n.-15G>A | |
NR_046072.1:n.18G>A | ||
XR_001745842.1:n.1312+14154C>T | ||
NM_006167.4:c.-15G>A MANE Select | NP_006158.2:n.-15G>A | |
NR_046072.2:n.35G>A |