HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20589007G>T , CM000686.2:g.20589007G>T | GRCh38 |
NC_000024.9:g.22750893G>T , CM000686.1:g.22750893G>T | GRCh37 |
NC_000024.8:g.21160281G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361365.7:c.338-477G>T MANE Select | ENSP00000354722.2:n.338-477G>T | |
ENST00000361365.6:c.338-477G>T | ENSP00000354722.2:n.338-477G>T | |
ENST00000382772.3:c.287-477G>T | ENSP00000372222.3:n.287-477G>T | |
ENST00000464196.5:n.2290G>T | ||
ENST00000485584.1:n.260-477G>T | ||
NM_001278612.1:c.287-477G>T | NP_001265541.1:n.287-477G>T | |
NM_004681.3:c.338-477G>T | NP_004672.2:n.338-477G>T | |
NM_004681.4:c.338-477G>T MANE Select | NP_004672.2:n.338-477G>T | |
NM_001278612.2:c.287-477G>T | NP_001265541.1:n.287-477G>T |