HGVS | Genome Assembly |
---|---|
NC_000002.12:g.113114474G>A , CM000664.2:g.113114474G>A | GRCh38 |
NC_000002.11:g.113872051G>A , CM000664.1:g.113872051G>A | GRCh37 |
NC_000002.10:g.113588522G>A | NCBI36 |
NG_021240.1:g.1582G>A , LRG_188:g.1582G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409052.6:c.-273+1360G>A | ENSP00000387210.1:n.-273+1360G>A | |
ENST00000463073.6:n.303-1031G>A | ||
ENST00000465812.6:n.646+1360G>A | ||
ENST00000409052.5:c.-273+1360G>A | ENSP00000387210.1:n.-273+1360G>A | |
ENST00000463073.5:n.200-1031G>A | ||
ENST00000465812.5:n.371+1360G>A | ||
XM_011511121.1:c.-273+1360G>A | XP_011509423.1:n.-273+1360G>A |