HGVS | Genome Assembly |
---|---|
NC_000010.11:g.119651659G>T , CM000672.2:g.119651659G>T | GRCh38 |
NC_000010.10:g.121411171G>T , CM000672.1:g.121411171G>T | GRCh37 |
NC_000010.9:g.121401161G>T | NCBI36 |
NG_016125.1:g.5290G>T , LRG_742:g.5290G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369085.8:c.-17G>T MANE Select | ENSP00000358081.4:n.-17G>T | |
ENST00000369085.7:c.-17G>T | ENSP00000358081.3:n.-17G>T | |
NM_004281.3:c.-17G>T , LRG_742t1:c.-17G>T | NP_004272.2:n.-17G>T | |
XM_005270287.1:c.-17G>T | XP_005270344.1:n.-17G>T | |
XM_005270287.2:c.-17G>T | XP_005270344.1:n.-17G>T | |
NM_004281.4:c.-17G>T MANE Select | NP_004272.2:n.-17G>T |