HGVS | Genome Assembly |
---|---|
NC_000002.12:g.71124456C= , CM000664.2:g.71124456C= | GRCh38 |
NC_000002.11:g.71351586C= , CM000664.1:g.71351586C= | GRCh37 |
NC_000002.10:g.71205094C= | NCBI36 |
NG_008977.1:g.10809G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000244217.6:c.128G= MANE Select | ENSP00000244217.5:p.Trp43= | |
ENST00000244217.5:c.128G= | ENSP00000244217.5:p.Trp43= | |
ENST00000486135.1:c.-158G= | ENSP00000441569.1:n.-158G= | |
ENST00000494660.6:c.-158G= | ENSP00000437361.1:n.-158G= | |
NM_032601.3:c.128G= | NP_115990.3:p.Trp43= | |
XM_005264613.2:c.128G= | XP_005264670.1:p.Trp43= | |
XR_939729.1:n.197G= | ||
XR_939729.2:n.197G= | ||
NM_032601.4:c.128G= MANE Select | NP_115990.3:p.Trp43= |