HGVS | Genome Assembly |
---|---|
NC_000002.12:g.217445669C>T , CM000664.2:g.217445669C>T | GRCh38 |
NC_000002.11:g.218310392C>T , CM000664.1:g.218310392C>T | GRCh37 |
NC_000002.10:g.218018637C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000474063.5:n.500-11553G>A | ||
ENST00000486365.5:n.1523-11553G>A | ||
NR_026597.1:n.1523-11553G>A | ||
NR_026597.2:n.1523-11553G>A |