HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071903G= , CM000667.2:g.111071903G= | GRCh38 |
NC_000005.9:g.110407601G= , CM000667.1:g.110407601G= | GRCh37 |
NC_000005.8:g.110435500G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.13G= MANE Select | ENSP00000339804.3:p.Ala5= | |
ENST00000344895.3:c.13G= | ENSP00000339804.3:p.Ala5= | |
ENST00000420978.6:c.35-22G= | ENSP00000399099.2:n.35-22G= | |
NM_033035.4:c.13G= | NP_149024.1:p.Ala5= | |
NR_045089.1:n.1439-22G= | ||
NM_033035.5:c.13G= MANE Select | NP_149024.1:p.Ala5= | |
NR_045089.2:n.1457-22G= |