HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659733T= , CM000683.2:g.31659733T= | GRCh38 |
NC_000021.8:g.33032046T= , CM000683.1:g.33032046T= | GRCh37 |
NC_000021.7:g.31953917T= | NCBI36 |
NG_008689.1:g.5112T= , LRG_652:g.5112T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.-37T= MANE Select | ENSP00000270142.7:n.-37T= | |
ENST00000270142.10:c.-37T= | ENSP00000270142.6:n.-37T= | |
ENST00000389995.4:c.-37T= | ENSP00000374645.4:n.-37T= | |
ENST00000470944.1:n.25T= | ||
ENST00000476106.5:n.41T= | ||
NM_000454.4:c.-37T= , LRG_652t1:c.-37T= | NP_000445.1:n.-37T= | |
NM_000454.5:c.-37T= MANE Select | NP_000445.1:n.-37T= |