HGVS | Genome Assembly |
---|---|
NC_000002.12:g.168900844C>T , CM000664.2:g.168900844C>T | GRCh38 |
NC_000002.11:g.169757354C>T , CM000664.1:g.169757354C>T | GRCh37 |
NC_000002.10:g.169465600C>T | NCBI36 |
NG_011682.1:g.4605C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000451987.5:c.-172-10158G>A | ENSP00000393322.1:n.-172-10158G>A | |
ENST00000472216.2:n.177-10158G>A |