HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7527499T= , CM000681.2:g.7527499T= | GRCh38 |
NC_000019.9:g.7592385T= , CM000681.1:g.7592385T= | GRCh37 |
NC_000019.8:g.7498385T= | NCBI36 |
NG_015806.1:g.9890T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.572-21T= MANE Select | ENSP00000264079.5:n.572-21T= | |
ENST00000264079.10:c.572-21T= | ENSP00000264079.5:n.572-21T= | |
ENST00000394321.9:n.652-21T= | ||
ENST00000598406.1:n.393-21T= | ||
ENST00000601003.1:c.572-365T= | ENSP00000469074.1:n.572-365T= | |
NM_020533.2:c.572-21T= | NP_065394.1:n.572-21T= | |
NM_020533.3:c.572-21T= MANE Select | NP_065394.1:n.572-21T= |