HGVS | Genome Assembly |
---|---|
NC_000012.12:g.47908762C>T , CM000674.2:g.47908762C>T | GRCh38 |
NC_000012.11:g.48302545C>T , CM000674.1:g.48302545C>T | GRCh37 |
NC_000012.10:g.46588812C>T | NCBI36 |
NG_008731.1:g.1270G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000395324.6:c.-83-25988G>A | ENSP00000378734.2:n.-83-25988G>A |