HGVS | Genome Assembly |
---|---|
NC_000022.11:g.43928986G= , CM000684.2:g.43928986G= | GRCh38 |
NC_000022.10:g.44324866G= , CM000684.1:g.44324866G= | GRCh37 |
NC_000022.9:g.42656199G= | NCBI36 |
NG_008631.1:g.10248G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000216180.8:c.486+97G= MANE Select | ENSP00000216180.3:n.486+97G= | |
ENST00000216180.7:c.486+97G= | ENSP00000216180.3:n.486+97G= | |
ENST00000406117.6:c.*118+97G= | ENSP00000384668.2:n.*118+97G= | |
ENST00000423180.2:c.474+97G= | ENSP00000397987.2:n.474+97G= | |
ENST00000478713.1:n.520+97G= | ||
NM_025225.2:c.486+97G= | NP_079501.2:n.486+97G= | |
NM_025225.3:c.486+97G= MANE Select | NP_079501.2:n.486+97G= |