HGVS | Genome Assembly |
---|---|
NC_000002.12:g.191014706C>T , CM000664.2:g.191014706C>T | GRCh38 |
NC_000002.11:g.191879432C>T , CM000664.1:g.191879432C>T | GRCh37 |
NC_000002.10:g.191587677C>T | NCBI36 |
NG_008294.1:g.4545G>A , LRG_111:g.4545G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000432058.1:c.-155-1028G>A | ENSP00000416019.1:n.-155-1028G>A | |
ENST00000454414.5:c.-1-4702G>A | ENSP00000411398.1:n.-1-4702G>A |