HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6722599T>A , CM000681.2:g.6722599T>A | GRCh38 |
NC_000019.9:g.6722610T>A , CM000681.1:g.6722610T>A | GRCh37 |
NC_000019.8:g.6673610T>A | NCBI36 |
NG_009557.1:g.3053A>T , LRG_27:g.3053A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000600744.1:c.-50+842A>T | ENSP00000472044.1:n.-50+842A>T |