HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32474910G>T , CM000684.2:g.32474910G>T | GRCh38 |
NC_000022.10:g.32870897G>T , CM000684.1:g.32870897G>T | GRCh37 |
NC_000022.9:g.31200897G>T | NCBI36 |
NG_016001.1:g.5191G>T | |
NG_016001.2:g.5191G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266087.12:c.-93G>T MANE Select | ENSP00000266087.7:n.-93G>T | |
ENST00000266087.11:c.-93G>T | ENSP00000266087.7:n.-93G>T | |
ENST00000420700.5:c.-93G>T | ENSP00000406155.1:n.-93G>T | |
ENST00000425028.5:c.-93G>T | ENSP00000395823.1:n.-93G>T | |
NM_012179.3:c.-93G>T | NP_036311.3:n.-93G>T | |
XM_011530106.1:c.-266G>T | XP_011528408.1:n.-266G>T | |
XM_024452207.1:c.-283G>T | XP_024307975.1:n.-283G>T | |
NM_012179.4:c.-93G>T MANE Select | NP_036311.3:n.-93G>T |