HGVS | Genome Assembly |
---|---|
NC_000006.12:g.28161967A>G , CM000668.2:g.28161967A>G | GRCh38 |
NC_000006.11:g.28129745A>G , CM000668.1:g.28129745A>G | GRCh37 |
NC_000006.10:g.28237724A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000562227.2:n.53+146A>G | ||
ENST00000440790.6:n.41+146A>G | ||
ENST00000570126.1:n.30+146A>G | ||
NR_103448.1:n.61+146A>G |