HGVS | Genome Assembly |
---|---|
NC_000010.11:g.46046395T>G , CM000672.2:g.46046395T>G | GRCh38 |
NC_000010.10:g.51549427A>C , CM000672.1:g.51549427A>C | GRCh37 |
NC_000010.9:g.51219433A>C | NCBI36 |
NG_011551.1:g.4875A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000663171.1:c.-142-16A>C | ENSP00000499419.1:n.-142-16A>C |