HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240576188G>A , CM000664.2:g.240576188G>A | GRCh38 |
NC_000002.11:g.241515605G>A , CM000664.1:g.241515605G>A | GRCh37 |
NC_000002.10:g.241164278G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270357.10:c.1511-347G>A MANE Select | ENSP00000270357.4:n.1511-347G>A | |
ENST00000270357.8:c.818-347G>A | ENSP00000270357.3:n.818-347G>A | |
ENST00000437406.1:c.110-380G>A | ENSP00000403319.1:n.110-380G>A | |
ENST00000451363.5:c.152-347G>A | ENSP00000414661.1:n.152-347G>A | |
ENST00000464550.5:n.347-347G>A | ||
ENST00000471657.1:n.314-347G>A | ||
ENST00000481757.5:n.2098G>A | ||
ENST00000486058.5:n.1624-347G>A | ||
ENST00000493398.5:n.657-347G>A | ||
NM_018226.4:c.1511-347G>A | NP_060696.4:n.1511-347G>A | |
XM_005247036.3:c.1511-380G>A | XP_005247093.1:n.1511-380G>A | |
NM_018226.5:c.1511-347G>A | NP_060696.4:n.1511-347G>A | |
XM_005247036.4:c.1511-380G>A | XP_005247093.1:n.1511-380G>A | |
NM_018226.6:c.1511-347G>A MANE Select | NP_060696.4:n.1511-347G>A |