HGVS | Genome Assembly |
---|---|
NC_000018.10:g.54174021T>G , CM000680.2:g.54174021T>G | GRCh38 |
NC_000018.9:g.51700391T>G , CM000680.1:g.51700391T>G | GRCh37 |
NC_000018.8:g.49954389T>G | NCBI36 |
NG_029550.1:g.55768A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256429.8:c.841-7855A>C MANE Select | ENSP00000256429.3:n.841-7855A>C | |
ENST00000256429.7:c.841-7855A>C | ENSP00000256429.3:n.841-7855A>C | |
ENST00000578272.1:c.287-7855A>C | ENSP00000462393.1:n.287-7855A>C | |
NM_003927.4:c.841-7855A>C | NP_003918.1:n.841-7855A>C | |
NM_003927.5:c.841-7855A>C MANE Select | NP_003918.1:n.841-7855A>C |