HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140114123C>T , CM000667.2:g.140114123C>T | GRCh38 |
NC_000005.9:g.139493708C>T , CM000667.1:g.139493708C>T | GRCh37 |
NC_000005.8:g.139473892C>T | NCBI36 |
NG_041813.1:g.5001C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331327.5:c.-59C>T MANE Select | ENSP00000332706.3:n.-59C>T | |
ENST00000505703.2:c.-59C>T | ENSP00000498560.1:n.-59C>T | |
ENST00000651386.1:c.-59C>T | ENSP00000499133.1:n.-59C>T | |
ENST00000331327.4:c.-59C>T | ENSP00000332706.3:n.-59C>T | |
ENST00000502351.1:n.365C>T | ||
ENST00000505703.1:n.407C>T | ||
NM_005859.4:c.-59C>T | NP_005850.1:n.-59C>T | |
NM_005859.5:c.-59C>T MANE Select | NP_005850.1:n.-59C>T |