HGVS | Genome Assembly |
---|---|
NC_000006.12:g.118252898G>A , CM000668.2:g.118252898G>A | GRCh38 |
NC_000006.11:g.118574061G>A , CM000668.1:g.118574061G>A | GRCh37 |
NC_000006.10:g.118680754G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360388.9:c.478-14097G>A MANE Select | ENSP00000353557.4:n.478-14097G>A | |
ENST00000360388.8:c.478-14097G>A | ENSP00000353557.4:n.478-14097G>A | |
ENST00000621341.1:c.301-14097G>A | ENSP00000484738.1:n.301-14097G>A | |
NM_001029858.3:c.478-14097G>A | NP_001025029.2:n.478-14097G>A | |
XM_005266865.3:c.478-14097G>A | XP_005266922.1:n.478-14097G>A | |
XM_005266865.4:c.478-14097G>A | XP_005266922.1:n.478-14097G>A | |
NM_001029858.4:c.478-14097G>A MANE Select | NP_001025029.2:n.478-14097G>A |