HGVS | Genome Assembly |
---|---|
NC_000002.12:g.191014614C>T , CM000664.2:g.191014614C>T | GRCh38 |
NC_000002.11:g.191879340C>T , CM000664.1:g.191879340C>T | GRCh37 |
NC_000002.10:g.191587585C>T | NCBI36 |
NG_008294.1:g.4637G>A , LRG_111:g.4637G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000432058.1:c.-155-936G>A | ENSP00000416019.1:n.-155-936G>A | |
ENST00000454414.5:c.-1-4610G>A | ENSP00000411398.1:n.-1-4610G>A |