HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20188924C>A , CM000675.2:g.20188924C>A | GRCh38 |
NC_000013.10:g.20763063C>A , CM000675.1:g.20763063C>A | GRCh37 |
NC_000013.9:g.19661063C>A | NCBI36 |
NG_008358.1:g.9052G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.658G>T | ENSP00000372295.1:p.Gly220Trp | |
ENST00000382848.5:c.658G>T MANE Select | ENSP00000372299.4:p.Gly220Trp | |
ENST00000382844.1:c.658G>T | ENSP00000372295.1:p.Gly220Trp | |
ENST00000382848.4:c.658G>T | ENSP00000372299.4:p.Gly220Trp | |
NM_004004.5:c.658G>T | NP_003995.2:p.Gly220Trp | |
XM_011535049.1:c.658G>T | XP_011533351.1:p.Gly220Trp | |
XM_011535049.2:c.658G>T | XP_011533351.1:p.Gly220Trp | |
NM_004004.6:c.658G>T MANE Select | NP_003995.2:p.Gly220Trp |