HGVS | Genome Assembly |
---|---|
NC_000019.10:g.41354391A= , CM000681.2:g.41354391A= | GRCh38 |
NC_000019.9:g.41860296A= , CM000681.1:g.41860296A= | GRCh37 |
NC_000019.8:g.46552136A= | NCBI36 |
NG_013091.1:g.14783T= | |
NG_013364.1:g.4536T= |
HGVS | Amino-acid Change |
---|---|
ENST00000539627.5:c.-30+3189A= | ENSP00000441900.1:n.-30+3189A= |
ENST00000604123.5:c.142+76A= | ENSP00000474871.1:n.142+76A= |
ENST00000604424.1:n.350+3189A= |