HGVS | Genome Assembly |
---|---|
NC_000023.11:g.68829666G>T , CM000685.2:g.68829666G>T | GRCh38 |
NC_000023.10:g.68049509G>T , CM000685.1:g.68049509G>T | GRCh37 |
NC_000023.9:g.67966234G>T | NCBI36 |
NG_008887.1:g.5670G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000204961.5:c.-111G>T MANE Select | ENSP00000204961.4:n.-111G>T | |
ENST00000204961.4:c.-111G>T | ENSP00000204961.4:n.-111G>T | |
NM_004429.4:c.-111G>T | NP_004420.1:n.-111G>T | |
NM_004429.5:c.-111G>T MANE Select | NP_004420.1:n.-111G>T |