HGVS | Genome Assembly |
---|---|
NC_000003.12:g.190404695A= , CM000665.2:g.190404695A= | GRCh38 |
NC_000003.11:g.190122484A= , CM000665.1:g.190122484A= | GRCh37 |
NC_000003.10:g.191605178A= | NCBI36 |
NG_008149.1:g.21644A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264734.3:c.218-67A= MANE Select | ENSP00000264734.3:n.218-67A= | |
ENST00000456423.2:c.115-5208A= | ENSP00000414136.2:n.115-5208A= | |
ENST00000264734.2:c.428-67A= | ENSP00000264734.2:n.428-67A= | |
ENST00000456423.1:c.325-5208A= | ENSP00000414136.1:n.325-5208A= | |
ENST00000468220.1:n.410-67A= | ||
NM_006580.3:c.428-67A= | NP_006571.1:n.428-67A= | |
NM_001378492.1:c.218-67A= | NP_001365421.1:n.218-67A= | |
NM_001378493.1:c.218-67A= | NP_001365422.1:n.218-67A= | |
NM_006580.4:c.218-67A= MANE Select | NP_006571.2:n.218-67A= |