HGVS | Genome Assembly |
---|---|
NC_000016.10:g.2340762G>T , CM000678.2:g.2340762G>T | GRCh38 |
NC_000016.9:g.2390763G>T , CM000678.1:g.2390763G>T | GRCh37 |
NC_000016.8:g.2330764G>T | NCBI36 |
NG_011790.1:g.4985C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000640929.1:n.42+1431G>T | ||
ENST00000512848.5:n.182+1431G>T |