HGVS | Genome Assembly |
---|---|
NC_000003.12:g.119413498A= , CM000665.2:g.119413498A= | GRCh38 |
NC_000003.11:g.119132345A= , CM000665.1:g.119132345A= | GRCh37 |
NC_000003.10:g.120615035A= | NCBI36 |
NG_007665.2:g.124126A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264245.9:c.1927-358A= MANE Select | ENSP00000264245.4:n.1927-358A= | |
ENST00000264245.8:c.1927-358A= | ENSP00000264245.4:n.1927-358A= | |
NM_020754.3:c.1927-358A= | NP_065805.2:n.1927-358A= | |
XM_005247671.3:c.1834-358A= | XP_005247728.1:n.1834-358A= | |
XM_006713714.2:c.1867-358A= | XP_006713777.1:n.1867-358A= | |
XM_006713714.3:c.1867-358A= | XP_006713777.1:n.1867-358A= | |
XM_017006955.1:c.1435-358A= | XP_016862444.1:n.1435-358A= | |
NM_020754.4:c.1927-358A= MANE Select | NP_065805.2:n.1927-358A= |