HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659637G>T , CM000683.2:g.31659637G>T | GRCh38 |
NC_000021.8:g.33031950G>T , CM000683.1:g.33031950G>T | GRCh37 |
NC_000021.7:g.31953821G>T | NCBI36 |
NG_008689.1:g.5016G>T , LRG_652:g.5016G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.10:c.-133G>T | ENSP00000270142.6:n.-133G>T | |
NM_000454.4:c.-133G>T , LRG_652t1:c.-133G>T | NP_000445.1:n.-133G>T |