HGVS | Genome Assembly |
---|---|
NC_000006.12:g.28162032C>A , CM000668.2:g.28162032C>A | GRCh38 |
NC_000006.11:g.28129810C>A , CM000668.1:g.28129810C>A | GRCh37 |
NC_000006.10:g.28237789C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000562227.2:n.53+211C>A | ||
ENST00000440790.6:n.41+211C>A | ||
ENST00000570126.1:n.30+211C>A | ||
NR_103448.1:n.61+211C>A |