HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44374665T= , CM000679.2:g.44374665T= | GRCh38 |
NC_000017.10:g.42452033T= , CM000679.1:g.42452033T= | GRCh37 |
NC_000017.9:g.39807559T= | NCBI36 |
NG_008331.1:g.19841A= , LRG_479:g.19841A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262407.6:c.2937A= MANE Select | ENSP00000262407.5:p.Glu979= | |
ENST00000648408.1:c.2368A= | ||
ENST00000262407.5:c.2937A= | ENSP00000262407.5:p.Glu979= | |
ENST00000587295.5:c.253+1168A= | ||
ENST00000588098.1:c.31A= | ||
ENST00000592462.5:n.2448A= | ||
NM_000419.3:c.2937A= , LRG_479t1:c.2937A= | NP_000410.2:p.Glu979= | |
XM_011524749.1:c.2842-195A= | XP_011523051.1:n.2842-195A= | |
XM_011524750.1:c.2937A= | XP_011523052.1:p.Glu979= | |
NM_000419.4:c.2937A= | NP_000410.2:p.Glu979= | |
NM_000419.5:c.2937A= MANE Select | NP_000410.2:p.Glu979= |