HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189059141T= , CM000664.2:g.189059141T= | GRCh38 |
NC_000002.11:g.189923867T= , CM000664.1:g.189923867T= | GRCh37 |
NC_000002.10:g.189632112T= | NCBI36 |
NG_011799.1:g.125739A= | |
NG_011799.2:g.125739A= | |
NG_011799.3:g.171161A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.2086-248A= MANE Select | ENSP00000364000.3:n.2086-248A= | |
ENST00000374866.7:c.2086-248A= | ENSP00000364000.3:n.2086-248A= | |
ENST00000470524.2:n.192-248A= | ||
ENST00000618828.1:c.925-248A= | ENSP00000482184.1:n.925-248A= | |
NM_000393.3:c.2086-248A= | NP_000384.2:n.2086-248A= | |
XM_011510573.1:c.1948-248A= | XP_011508875.1:n.1948-248A= | |
NM_000393.4:c.2086-248A= | NP_000384.2:n.2086-248A= | |
XM_011510573.3:c.1948-248A= | XP_011508875.1:n.1948-248A= | |
NM_000393.5:c.2086-248A= MANE Select | NP_000384.2:n.2086-248A= |