HGVS | Genome Assembly |
---|---|
NC_000011.10:g.128891545T>C , CM000673.2:g.128891545T>C | GRCh38 |
NC_000011.9:g.128761440T>C , CM000673.1:g.128761440T>C | GRCh37 |
NC_000011.8:g.128266650T>C | NCBI36 |
NG_023406.2:g.5128T>C , LRG_333:g.5128T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000529694.6:c.-187T>C MANE Select | ENSP00000433295.1:n.-187T>C | |
ENST00000338350.4:c.-276T>C | ENSP00000339960.4:n.-276T>C | |
ENST00000529694.5:c.-187T>C | ENSP00000433295.1:n.-187T>C | |
NM_000890.3:c.-187T>C , LRG_333t1:c.-187T>C | NP_000881.3:n.-187T>C | |
NM_000890.4:c.-187T>C | NP_000881.3:n.-187T>C | |
NM_001354169.1:c.-276T>C | NP_001341098.1:n.-276T>C | |
NM_000890.5:c.-187T>C MANE Select | NP_000881.3:n.-187T>C | |
NM_001354169.2:c.-276T>C | NP_001341098.1:n.-276T>C |