HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7530047T= , CM000681.2:g.7530047T= | GRCh38 |
NC_000019.9:g.7594933T= , CM000681.1:g.7594933T= | GRCh37 |
NC_000019.8:g.7500933T= | NCBI36 |
NG_013374.1:g.896T= | |
NG_015806.1:g.12438T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.1360-239T= MANE Select | ENSP00000264079.5:n.1360-239T= | |
ENST00000264079.10:c.1360-239T= | ENSP00000264079.5:n.1360-239T= | |
ENST00000394321.9:n.1675-239T= | ||
ENST00000594692.1:n.356-239T= | ||
ENST00000595860.5:n.543-239T= | ||
ENST00000599334.1:c.236+335T= | ||
NM_020533.2:c.1360-239T= | NP_065394.1:n.1360-239T= | |
NM_020533.3:c.1360-239T= MANE Select | NP_065394.1:n.1360-239T= |