HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104850205G>A , CM000672.2:g.104850205G>A | GRCh38 |
NC_000010.10:g.106609963G>A , CM000672.1:g.106609963G>A | GRCh37 |
NC_000010.9:g.106599953G>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369701.8:c.695+7346G>A MANE Select | ENSP00000358715.3:n.695+7346G>A | |
ENST00000369699.8:c.695+7346G>A | ENSP00000358713.5:n.695+7346G>A | |
ENST00000369701.7:c.695+7346G>A | ENSP00000358715.3:n.695+7346G>A | |
NM_014978.2:c.695+7346G>A | NP_055793.1:n.695+7346G>A | |
XM_011539541.1:c.695+7346G>A | XP_011537843.1:n.695+7346G>A | |
NM_014978.3:c.695+7346G>A MANE Select | NP_055793.1:n.695+7346G>A |