HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6709959T= , CM000681.2:g.6709959T= | GRCh38 |
NC_000019.9:g.6709970T= , CM000681.1:g.6709970T= | GRCh37 |
NC_000019.8:g.6660970T= | NCBI36 |
NG_009557.1:g.15693A= , LRG_27:g.15693A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.1564-117A= | ENSP00000512083.1:n.1564-117A= | |
ENST00000695654.1:c.811-117A= | ENSP00000512085.1:n.811-117A= | |
ENST00000695655.1:c.592-81A= | ENSP00000512086.1:n.592-81A= | |
ENST00000695692.1:n.1051-117A= | ||
ENST00000245907.11:c.1687-117A= MANE Select | ENSP00000245907.4:n.1687-117A= | |
ENST00000245907.10:c.1687-117A= | ENSP00000245907.4:n.1687-117A= | |
ENST00000600763.1:n.320-117A= | ||
NM_000064.3:c.1687-117A= | NP_000055.2:n.1687-117A= | |
NM_000064.4:c.1687-117A= MANE Select | NP_000055.2:n.1687-117A= |