HGVS | Genome Assembly |
---|---|
NC_000005.10:g.157110523C>T , CM000667.2:g.157110523C>T | GRCh38 |
NC_000005.9:g.156537534C>T , CM000667.1:g.156537534C>T | GRCh37 |
NC_000005.8:g.156470112C>T | NCBI36 |
NG_030444.1:g.3715G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000524219.2:c.-293-3561G>A | ENSP00000430328.2:n.-293-3561G>A | |
ENST00000696899.1:c.-264-1276G>A | ENSP00000512960.1:n.-264-1276G>A | |
ENST00000524219.1:c.-293-3561G>A | ENSP00000430328.1:n.-293-3561G>A |