HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071850A= , CM000667.2:g.111071850A= | GRCh38 |
NC_000005.9:g.110407548A= , CM000667.1:g.110407548A= | GRCh37 |
NC_000005.8:g.110435447A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.-41A= MANE Select | ENSP00000339804.3:n.-41A= | |
ENST00000344895.3:c.-41A= | ENSP00000339804.3:n.-41A= | |
ENST00000420978.6:c.35-75A= | ENSP00000399099.2:n.35-75A= | |
NM_033035.4:c.-41A= | NP_149024.1:n.-41A= | |
NR_045089.1:n.1439-75A= | ||
NM_033035.5:c.-41A= MANE Select | NP_149024.1:n.-41A= | |
NR_045089.2:n.1457-75A= |