HGVS | Genome Assembly |
---|---|
NC_000006.12:g.28161825T>A , CM000668.2:g.28161825T>A | GRCh38 |
NC_000006.11:g.28129603T>A , CM000668.1:g.28129603T>A | GRCh37 |
NC_000006.10:g.28237582T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000562227.2:n.53+4T>A | ||
ENST00000440790.6:n.41+4T>A | ||
ENST00000570126.1:n.30+4T>A | ||
NR_103448.1:n.61+4T>A |