HGVS | Genome Assembly |
---|---|
NC_000003.12:g.14125108A= , CM000665.2:g.14125108A= | GRCh38 |
NC_000003.11:g.14166608A= , CM000665.1:g.14166608A= | GRCh37 |
NC_000003.10:g.14141609A= | NCBI36 |
NG_008975.1:g.5169A= , LRG_435:g.5169A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000432444.2:c.-86A= | ENSP00000395617.1:n.-86A= | |
ENST00000306077.5:c.-86A= MANE Select | ENSP00000303992.5:n.-86A= | |
ENST00000306077.4:c.-86A= | ENSP00000303992.4:n.-86A= | |
ENST00000432444.1:c.-86A= | ENSP00000395617.1:n.-86A= | |
NM_024334.2:c.-86A= , LRG_435t1:c.-86A= | NP_077310.1:n.-86A= | |
XM_017007176.2:c.-422A= | XP_016862665.1:n.-422A= | |
NM_024334.3:c.-86A= MANE Select | NP_077310.1:n.-86A= |