HGVS | Genome Assembly |
---|---|
NC_000023.11:g.78123046G= , CM000685.2:g.78123046G= | GRCh38 |
NC_000023.10:g.77378543G= , CM000685.1:g.77378543G= | GRCh37 |
NC_000023.9:g.77265199G= | NCBI36 |
NG_008862.1:g.23878G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373316.5:c.756+97G= MANE Select | ENSP00000362413.4:n.756+97G= | |
ENST00000644362.1:c.672+97G= | ENSP00000496140.1:n.672+97G= | |
ENST00000373316.4:c.756+97G= | ENSP00000362413.4:n.756+97G= | |
ENST00000474281.1:n.163+45G= | ||
NM_000291.3:c.756+97G= | NP_000282.1:n.756+97G= | |
NM_000291.4:c.756+97G= MANE Select | NP_000282.1:n.756+97G= |