HGVS | Genome Assembly |
---|---|
NC_000001.11:g.108875057C>A , CM000663.2:g.108875057C>A | GRCh38 |
NC_000001.10:g.109417679C>A , CM000663.1:g.109417679C>A | GRCh37 |
NC_000001.9:g.109219202C>A | NCBI36 |
NG_028108.1:g.3077C>A | |
NG_028108.2:g.4708C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000357393.6:c.1-25481G>T | ENSP00000349968.6:n.1-25481G>T | |
ENST00000357393.5:c.115-25481G>T | ENSP00000349968.5:n.115-25481G>T | |
XR_001738178.1:n.103+83G>T |