HGVS | Genome Assembly |
---|---|
NC_000002.12:g.223053441G>T , CM000664.2:g.223053441G>T | GRCh38 |
NC_000002.11:g.223918159G>T , CM000664.1:g.223918159G>T | GRCh37 |
NC_000002.10:g.223626403G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000281830.4:c.*98G>T MANE Select | ENSP00000281830.5:n.*98G>T | |
ENST00000281830.3:c.*98G>T | ENSP00000281830.4:n.*98G>T | |
ENST00000488477.2:n.75+1167G>T | ||
NM_080671.3:c.*98G>T | NP_542402.3:n.*98G>T | |
NM_080671.4:c.*98G>T MANE Select | NP_542402.4:n.*98G>T |