HGVS | Genome Assembly |
---|---|
NC_000008.11:g.42732624A= , CM000670.2:g.42732624A= | GRCh38 |
NC_000008.10:g.42587767A= , CM000670.1:g.42587767A= | GRCh37 |
NC_000008.9:g.42706924A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000289957.3:c.1242+75A= MANE Select | ENSP00000289957.2:n.1242+75A= | |
ENST00000289957.2:c.1242+75A= | ENSP00000289957.2:n.1242+75A= | |
NM_000749.3:c.1242+75A= | NP_000740.1:n.1242+75A= | |
XM_011544390.1:c.855+75A= | XP_011542692.1:n.855+75A= | |
NM_000749.4:c.1242+75A= | NP_000740.1:n.1242+75A= | |
NM_001347717.1:c.1020+75A= | NP_001334646.1:n.1020+75A= | |
XM_011544390.2:c.855+75A= | XP_011542692.1:n.855+75A= | |
NM_000749.5:c.1242+75A= MANE Select | NP_000740.1:n.1242+75A= | |
NM_001347717.2:c.1020+75A= | NP_001334646.1:n.1020+75A= |