HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32177662A= , CM000668.2:g.32177662A= | GRCh38 |
NC_000006.11:g.32145439A= , CM000668.1:g.32145439A= | GRCh37 |
NC_000006.10:g.32253417A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000336984.6:c.-10+339T= | ENSP00000337463.6:n.-10+339T= | |
ENST00000395497.5:c.-128T= | ENSP00000378875.1:n.-128T= | |
NM_032741.4:c.-10+339T= | NP_116130.2:n.-10+339T= | |
XM_011514234.1:c.-128T= | XP_011512536.1:n.-128T= | |
XM_005248806.2:c.-438T= | XP_005248863.1:n.-438T= | |
NM_032741.5:c.-10+339T= | NP_116130.2:n.-10+339T= |