HGVS | Genome Assembly |
---|---|
NC_000002.12:g.135789549C= , CM000664.2:g.135789549C= | GRCh38 |
NC_000002.11:g.136547119C= , CM000664.1:g.136547119C= | GRCh37 |
NC_000002.10:g.136263589C= | NCBI36 |
NG_008104.2:g.70621G= , LRG_338:g.70621G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264162.7:c.5563+22G= MANE Select | ENSP00000264162.2:n.5563+22G= | |
ENST00000264162.6:c.5563+22G= | ENSP00000264162.2:n.5563+22G= | |
NM_002299.2:c.5563+22G= , LRG_338t1:c.5563+22G= | NP_002290.2:n.5563+22G= | |
NM_002299.3:c.5563+22G= | NP_002290.2:n.5563+22G= | |
NM_002299.4:c.5563+22G= MANE Select | NP_002290.2:n.5563+22G= |