HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659739G>A , CM000683.2:g.31659739G>A | GRCh38 |
NC_000021.8:g.33032052G>A , CM000683.1:g.33032052G>A | GRCh37 |
NC_000021.7:g.31953923G>A | NCBI36 |
NG_008689.1:g.5118G>A , LRG_652:g.5118G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.-31G>A MANE Select | ENSP00000270142.7:n.-31G>A | |
ENST00000270142.10:c.-31G>A | ENSP00000270142.6:n.-31G>A | |
ENST00000389995.4:c.-31G>A | ENSP00000374645.4:n.-31G>A | |
ENST00000470944.1:n.31G>A | ||
ENST00000476106.5:n.47G>A | ||
NM_000454.4:c.-31G>A , LRG_652t1:c.-31G>A | NP_000445.1:n.-31G>A | |
NM_000454.5:c.-31G>A MANE Select | NP_000445.1:n.-31G>A |