HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659790C>T , CM000683.2:g.31659790C>T | GRCh38 |
NC_000021.8:g.33032103C>T , CM000683.1:g.33032103C>T | GRCh37 |
NC_000021.7:g.31953974C>T | NCBI36 |
NG_008689.1:g.5169C>T , LRG_652:g.5169C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.21C>T MANE Select | ENSP00000270142.7:p.Cys7= | |
ENST00000270142.10:c.21C>T | ENSP00000270142.6:p.Cys7= | |
ENST00000389995.4:c.15+6C>T | ENSP00000374645.4:n.15+6C>T | |
ENST00000470944.1:n.82C>T | ||
ENST00000476106.5:n.98C>T | ||
NM_000454.4:c.21C>T , LRG_652t1:c.21C>T | NP_000445.1:p.Cys7= | |
NM_000454.5:c.21C>T MANE Select | NP_000445.1:p.Cys7= |