HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55125461G>A , CM000666.2:g.55125461G>A | GRCh38 |
NC_000004.11:g.55991628G>A , CM000666.1:g.55991628G>A | GRCh37 |
NC_000004.10:g.55686385G>A | NCBI36 |
NG_012004.1:g.5135C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.-168C>T MANE Select | ENSP00000263923.4:n.-168C>T | |
ENST00000263923.4:c.-168C>T | ENSP00000263923.4:n.-168C>T | |
NM_002253.2:c.-168C>T | NP_002244.1:n.-168C>T | |
NM_002253.3:c.-168C>T | NP_002244.1:n.-168C>T | |
NM_002253.4:c.-168C>T MANE Select | NP_002244.1:n.-168C>T |