HGVS | Genome Assembly |
---|---|
NC_000002.12:g.79405076A>T , CM000664.2:g.79405076A>T | GRCh38 |
NC_000002.11:g.79632202A>T , CM000664.1:g.79632202A>T | GRCh37 |
NC_000002.10:g.79485710A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000466387.5:c.-135+31063A>T | ENSP00000418191.1:n.-135+31063A>T | |
NM_001399737.1:c.-135+31063A>T | NP_001386666.1:n.-135+31063A>T |