HGVS | Genome Assembly |
---|---|
NC_000006.12:g.43929990C>T , CM000668.2:g.43929990C>T | GRCh38 |
NC_000006.11:g.43897727C>T , CM000668.1:g.43897727C>T | GRCh37 |
NC_000006.10:g.44005705C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
NR_024478.1:n.439-6374C>T (LINC01512) | ||
NM_001318876.2:c.945+400719C>T (POLR1C) | NP_001305805.1:n.945+400719C>T |