HGVS | Genome Assembly |
---|---|
NC_000005.10:g.63962170T>G , CM000667.2:g.63962170T>G | GRCh38 |
NC_000005.9:g.63257997T>G , CM000667.1:g.63257997T>G | GRCh37 |
NC_000005.8:g.63293753T>G | NCBI36 |
NG_032816.1:g.5123A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000323865.5:c.-451A>C MANE Select | ENSP00000316244.4:n.-451A>C | |
ENST00000506598.1:c.-387-64A>C | ENSP00000423433.1:n.-387-64A>C | |
NM_000524.3:c.-451A>C | NP_000515.2:n.-451A>C | |
NM_000524.4:c.-451A>C MANE Select | NP_000515.2:n.-451A>C |