HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659623T>G , CM000683.2:g.31659623T>G | GRCh38 |
NC_000021.8:g.33031936T>G , CM000683.1:g.33031936T>G | GRCh37 |
NC_000021.7:g.31953807T>G | NCBI36 |
NG_008689.1:g.5002T>G , LRG_652:g.5002T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.10:c.-147T>G | ENSP00000270142.6:n.-147T>G | |
NM_000454.4:c.-147T>G , LRG_652t1:c.-147T>G | NP_000445.1:n.-147T>G |