HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240878714G= , CM000664.2:g.240878714G= | GRCh38 |
NC_000002.11:g.241818131G= , CM000664.1:g.241818131G= | GRCh37 |
NC_000002.10:g.241466804G= | NCBI36 |
NG_008005.1:g.14970G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000307503.4:c.1072G= MANE Select | ENSP00000302620.3:p.Val358= | |
ENST00000307503.3:c.1072G= | ENSP00000302620.3:p.Val358= | |
ENST00000470255.1:n.850G= | ||
NM_000030.2:c.1072G= | NP_000021.1:p.Val358= | |
NM_000030.3:c.1072G= MANE Select | NP_000021.1:p.Val358= |