HGVS | Genome Assembly |
---|---|
NC_000005.10:g.107646907A= , CM000667.2:g.107646907A= | GRCh38 |
NC_000005.9:g.106982608A= , CM000667.1:g.106982608A= | GRCh37 |
NC_000005.8:g.107010507A= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000333274.11:c.125+23582T= MANE Select | ENSP00000328777.6:n.125+23582T= | |
ENST00000333274.10:c.125+23582T= | ENSP00000328777.6:n.125+23582T= | |
ENST00000504941.1:n.397+23582T= | ||
ENST00000509503.1:c.125+23582T= | ENSP00000426989.1:n.125+23582T= | |
NM_001962.2:c.125+23582T= | NP_001953.1:n.125+23582T= | |
XM_006714565.1:c.125+23582T= | XP_006714628.1:n.125+23582T= | |
XM_006714565.3:c.125+23582T= | XP_006714628.1:n.125+23582T= | |
NM_001962.3:c.125+23582T= MANE Select | NP_001953.1:n.125+23582T= |