HGVS | Genome Assembly |
---|---|
NC_000008.11:g.8864774C= , CM000670.2:g.8864774C= | GRCh38 |
NC_000008.10:g.8722284C= , CM000670.1:g.8722284C= | GRCh37 |
NC_000008.9:g.8759694C= | NCBI36 |
NG_009444.1:g.33848G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000276282.7:c.2998+25287G= MANE Select | ENSP00000276282.6:n.2998+25287G= | |
ENST00000276282.6:c.2998+25287G= | ENSP00000276282.6:n.2998+25287G= | |
NM_004225.2:c.2998+25287G= | NP_004216.2:n.2998+25287G= | |
XR_246634.2:n.3534+25287G= | ||
XM_024447330.1:c.2998+25287G= | XP_024303098.1:n.2998+25287G= | |
NM_004225.3:c.2998+25287G= MANE Select | NP_004216.2:n.2998+25287G= |