HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6722554C>T , CM000681.2:g.6722554C>T | GRCh38 |
NC_000019.9:g.6722565C>T , CM000681.1:g.6722565C>T | GRCh37 |
NC_000019.8:g.6673565C>T | NCBI36 |
NG_009557.1:g.3098G>A , LRG_27:g.3098G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000600744.1:c.-50+887G>A | ENSP00000472044.1:n.-50+887G>A |