HGVS | Genome Assembly |
---|---|
NC_000006.12:g.28161899G>T , CM000668.2:g.28161899G>T | GRCh38 |
NC_000006.11:g.28129677G>T , CM000668.1:g.28129677G>T | GRCh37 |
NC_000006.10:g.28237656G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000562227.2:n.53+78G>T | ||
ENST00000440790.6:n.41+78G>T | ||
ENST00000570126.1:n.30+78G>T | ||
NR_103448.1:n.61+78G>T |