HGVS | Genome Assembly |
---|---|
NC_000019.10:g.47004080C>T , CM000681.2:g.47004080C>T | GRCh38 |
NC_000019.9:g.47507337C>T , CM000681.1:g.47507337C>T | GRCh37 |
NC_000019.8:g.52199177C>T | NCBI36 |
NG_047014.1:g.90514C>T | |
NG_047014.2:g.148084C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000404338.8:c.7892C>T | ENSP00000385720.2:n.7892C>T | |
ENST00000672722.1:c.*3392C>T MANE Select | ENSP00000500409.1:n.*3392C>T | |
ENST00000404338.7:c.7892C>T | ENSP00000385720.2:n.7892C>T | |
ENST00000614079.1:c.7469C>T | ENSP00000483730.1:n.7469C>T | |
NM_004491.4:c.7892C>T | NP_004482.4:n.7892C>T | |
NM_004491.5:c.*3392C>T MANE Select | NP_004482.4:n.*3392C>T |