HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44290937G= , CM000683.2:g.44290937G= | GRCh38 |
NC_000021.8:g.45710820G= , CM000683.1:g.45710820G= | GRCh37 |
NC_000021.7:g.44535248G= | NCBI36 |
NG_009556.1:g.10058G= , LRG_18:g.10058G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291582.6:c.880-158G= MANE Select | ENSP00000291582.5:n.880-158G= | |
ENST00000291582.5:c.880-158G= | ENSP00000291582.5:n.880-158G= | |
ENST00000337909.5:n.183G= | ||
ENST00000397994.8:n.183G= | ||
ENST00000527919.5:n.1613-161G= | ||
ENST00000530812.5:n.2630-161G= | ||
NM_000383.3:c.880-158G= | NP_000374.1:n.880-158G= | |
XM_011529551.1:c.880-161G= | XP_011527853.1:n.880-161G= | |
NM_000383.4:c.880-158G= MANE Select | NP_000374.1:n.880-158G= |