HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443940G>T , CM000668.2:g.32443940G>T | GRCh38 |
NC_000006.11:g.32411717G>T , CM000668.1:g.32411717G>T | GRCh37 |
NC_000006.10:g.32519695G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.*11+19G>T MANE Select | ENSP00000378786.2:n.*11+19G>T | |
ENST00000374982.5:c.*11+19G>T | ENSP00000364121.5:n.*11+19G>T | |
ENST00000395388.6:c.*11+19G>T | ENSP00000378786.2:n.*11+19G>T | |
NM_019111.4:c.*11+19G>T | NP_061984.2:n.*11+19G>T | |
NM_019111.5:c.*11+19G>T MANE Select | NP_061984.2:n.*11+19G>T |