HGVS | Genome Assembly |
---|---|
NC_000017.11:g.8076329C= , CM000679.2:g.8076329C= | GRCh38 |
NC_000017.10:g.7979647C= , CM000679.1:g.7979647C= | GRCh37 |
NC_000017.9:g.7920372C= | NCBI36 |
NG_007099.1:g.16375G= | |
NG_007099.2:g.16388G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647874.1:c.1378G= MANE Select | ENSP00000497784.1:p.Val460= | |
ENST00000649809.1:c.442G= | ENSP00000496845.1:p.Val148= | |
ENST00000319144.4:c.1378G= | ENSP00000315167.4:p.Val460= | |
ENST00000577351.5:n.325G= | ||
ENST00000583276.5:n.762G= | ||
ENST00000584116.1:n.634G= | ||
NM_001139.2:c.1378G= | NP_001130.1:p.Val460= | |
NM_001139.3:c.1378G= MANE Select | NP_001130.1:p.Val460= |