HGVS | Genome Assembly |
---|---|
NC_000002.12:g.162267514G= , CM000664.2:g.162267514G= | GRCh38 |
NC_000002.11:g.163124024G= , CM000664.1:g.163124024G= | GRCh37 |
NC_000002.10:g.162832270G= | NCBI36 |
NG_011495.1:g.56016C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000697291.1:c.*2460C= | ENSP00000513228.1:n.*2460C= | |
ENST00000648433.1:c.2746C= | ENSP00000496816.1:p.Gln916= | |
ENST00000649426.1:n.624C= | ||
ENST00000649554.1:n.2473C= | ||
ENST00000649979.2:c.2863C= MANE Select | ENSP00000497271.1:p.Gln955= | |
ENST00000679938.1:c.2551C= | ENSP00000505518.1:p.Gln851= | |
ENST00000263642.2:c.2863C= | ENSP00000263642.2:p.Gln955= | |
NM_022168.3:c.2863C= | NP_071451.2:p.Gln955= | |
XM_011511628.1:c.2146C= | XP_011509930.1:p.Gln716= | |
NM_022168.4:c.2863C= MANE Select | NP_071451.2:p.Gln955= |