HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240877566C= , CM000664.2:g.240877566C= | GRCh38 |
NC_000002.11:g.241816983C= , CM000664.1:g.241816983C= | GRCh37 |
NC_000002.10:g.241465656C= | NCBI36 |
NG_008005.1:g.13822C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.876C= MANE Select | ENSP00000302620.3:p.Arg292= | |
ENST00000307503.3:c.876C= | ENSP00000302620.3:p.Arg292= | |
ENST00000470255.1:n.654C= | ||
NM_000030.2:c.876C= | NP_000021.1:p.Arg292= | |
NM_000030.3:c.876C= MANE Select | NP_000021.1:p.Arg292= |