HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94426603T= , CM000669.2:g.94426603T= | GRCh38 |
NC_000007.13:g.94055915T= , CM000669.1:g.94055915T= | GRCh37 |
NC_000007.12:g.93893851T= | NCBI36 |
NG_007405.1:g.37043T= , LRG_2:g.37043T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297268.11:c.3105+73T= MANE Select | ENSP00000297268.6:n.3105+73T= | |
ENST00000297268.10:c.3105+73T= | ENSP00000297268.6:n.3105+73T= | |
ENST00000478215.1:n.737T= | ||
ENST00000481570.5:n.3151T= | ||
ENST00000488121.1:n.21+73T= | ||
ENST00000620463.1:c.3099+73T= | ENSP00000477719.1:n.3099+73T= | |
NM_000089.3:c.3105+73T= , LRG_2t1:c.3105+73T= | NP_000080.2:n.3105+73T= | |
NM_000089.4:c.3105+73T= MANE Select | NP_000080.2:n.3105+73T= |