HGVS | Genome Assembly |
---|---|
NC_000016.10:g.20353114A= , CM000678.2:g.20353114A= | GRCh38 |
NC_000016.9:g.20364436A= , CM000678.1:g.20364436A= | GRCh37 |
NC_000016.8:g.20271937A= | NCBI36 |
NG_008151.1:g.4602T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000570689.5:c.-39-2338T= | ENSP00000460548.1:n.-39-2338T= | |
XM_011545938.1:c.-39-2338T= | XP_011544240.1:n.-39-2338T= |