HGVS | Genome Assembly |
---|---|
NC_000002.12:g.218812709G>C , CM000664.2:g.218812709G>C | GRCh38 |
NC_000002.11:g.219677432G>C , CM000664.1:g.219677432G>C | GRCh37 |
NC_000002.10:g.219385676G>C | NCBI36 |
NG_007959.1:g.35961G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258415.9:c.804G>C MANE Select | ENSP00000258415.4:p.Trp268Cys | |
ENST00000258415.8:c.804G>C | ENSP00000258415.4:p.Trp268Cys | |
ENST00000411688.1:c.522G>C | ENSP00000392671.1:p.Trp174Cys | |
ENST00000445971.1:c.*265G>C | ENSP00000404945.1:n.*265G>C | |
ENST00000466602.1:n.752G>C | ||
ENST00000494263.5:n.1238G>C | ||
NM_000784.3:c.804G>C | NP_000775.1:p.Trp268Cys | |
XM_017003488.2:c.384G>C | XP_016858977.1:p.Trp128Cys | |
NM_000784.4:c.804G>C MANE Select | NP_000775.1:p.Trp268Cys |