HGVS | Genome Assembly |
---|---|
NC_000019.10:g.38930898T= , CM000681.2:g.38930898T= | GRCh38 |
NC_000019.9:g.39421538T= , CM000681.1:g.39421538T= | GRCh37 |
NC_000019.8:g.44113378T= | NCBI36 |
NG_029222.1:g.5191T= | |
NG_031865.1:g.4999A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308018.8:c.-120T= | ENSP00000308845.3:n.-120T= | |
ENST00000599996.1:c.476-4598A= | ||
NM_033362.3:c.-120T= | NP_203526.1:n.-120T= |