HGVS | Genome Assembly |
---|---|
NC_000007.14:g.150977834T= , CM000669.2:g.150977834T= | GRCh38 |
NC_000007.13:g.150674922T= , CM000669.1:g.150674922T= | GRCh37 |
NC_000007.12:g.150305855T= | NCBI36 |
NG_008916.1:g.5093A= , LRG_288:g.5093A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262186.10:c.76+4A= MANE Select | ENSP00000262186.5:n.76+4A= | |
ENST00000262186.9:c.76+4A= | ENSP00000262186.5:n.76+4A= | |
ENST00000430723.4:c.-102+4A= | ENSP00000387657.4:n.-102+4A= | |
ENST00000532957.5:n.299+4A= | ||
NM_000238.3:c.76+4A= , LRG_288t1:c.76+4A= | NP_000229.1:n.76+4A= | |
NM_172056.2:c.76+4A= , LRG_288t2:c.76+4A= | NP_742053.1:n.76+4A= | |
XM_011516186.1:c.76+4A= | XP_011514488.1:n.76+4A= | |
XM_011516186.3:c.76+4A= | XP_011514488.1:n.76+4A= | |
NM_000238.4:c.76+4A= MANE Select | NP_000229.1:n.76+4A= |