HGVS | Genome Assembly |
---|---|
NC_000001.11:g.15445531G= , CM000663.2:g.15445531G= | GRCh38 |
NC_000001.10:g.15772026G= , CM000663.1:g.15772026G= | GRCh37 |
NC_000001.9:g.15644613G= | NCBI36 |
NG_009253.1:g.12089G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375949.5:c.640-66G= MANE Select | ENSP00000365116.4:n.640-66G= | |
ENST00000375943.6:c.*94-66G= | ENSP00000365110.2:n.*94-66G= | |
ENST00000375949.4:c.640-66G= | ENSP00000365116.4:n.640-66G= | |
ENST00000483406.1:n.404-66G= | ||
NM_007272.2:c.640-66G= | NP_009203.2:n.640-66G= | |
XM_011540550.1:c.494-66G= | XP_011538852.1:n.494-66G= | |
NM_007272.3:c.640-66G= MANE Select | NP_009203.2:n.640-66G= |