HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32576575T>C , CM000668.2:g.32576575T>C | GRCh38 |
NC_000006.11:g.32544352T>C , CM000668.1:g.32544352T>C | GRCh37 |
NC_000006.10:g.32652330T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000611060.4:c.787+3672A>G | ENSP00000480667.1:n.787+3672A>G |