HGVS | Genome Assembly |
---|---|
NC_000003.12:g.49130825A= , CM000665.2:g.49130825A= | GRCh38 |
NC_000003.11:g.49168258A= , CM000665.1:g.49168258A= | GRCh37 |
NC_000003.10:g.49143262A= | NCBI36 |
NG_008094.1:g.7342T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000305544.9:c.951T= MANE Select | ENSP00000307156.4:p.Arg317= | |
ENST00000305544.8:c.951T= | ENSP00000307156.4:p.Arg317= | |
ENST00000418109.5:c.951T= | ENSP00000388325.1:p.Arg317= | |
NM_002292.3:c.951T= | NP_002283.3:p.Arg317= | |
XM_005265127.3:c.951T= | XP_005265184.1:p.Arg317= | |
XM_005265127.4:c.951T= | XP_005265184.1:p.Arg317= | |
NM_002292.4:c.951T= MANE Select | NP_002283.3:p.Arg317= |