HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128312570T= , CM000667.2:g.128312570T= | GRCh38 |
NC_000005.9:g.127648262T= , CM000667.1:g.127648262T= | GRCh37 |
NC_000005.8:g.127676161T= | NCBI36 |
NG_008750.1:g.230474A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703783.1:n.1663+64A= | ||
ENST00000703785.1:n.1583-617A= | ||
ENST00000262464.9:c.4879+64A= MANE Select | ENSP00000262464.4:n.4879+64A= | |
ENST00000262464.8:c.4879+64A= | ENSP00000262464.4:n.4879+64A= | |
ENST00000508053.5:c.4879+64A= | ENSP00000424571.1:n.4879+64A= | |
ENST00000619499.4:c.4876+64A= | ENSP00000482132.1:n.4876+64A= | |
NM_001999.3:c.4879+64A= | NP_001990.2:n.4879+64A= | |
XM_017009228.2:c.4726+64A= | XP_016864717.1:n.4726+64A= | |
NM_001999.4:c.4879+64A= MANE Select | NP_001990.2:n.4879+64A= |