HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110914322G>A , CM000674.2:g.110914322G>A | GRCh38 |
NC_000012.11:g.111352126G>A , CM000674.1:g.111352126G>A | GRCh37 |
NC_000012.10:g.109836509G>A | NCBI36 |
NG_007554.1:g.11256C>T , LRG_393:g.11256C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000228841.15:c.170-32C>T MANE Select | ENSP00000228841.8:n.170-32C>T | |
ENST00000663220.1:c.113-32C>T | ENSP00000499568.1:n.113-32C>T | |
ENST00000228841.12:c.170-32C>T | ENSP00000228841.7:n.170-32C>T | |
ENST00000548438.1:c.96C>T | ENSP00000447154.1:p.Leu32= | |
NM_000432.3:c.170-32C>T , LRG_393t1:c.170-32C>T | NP_000423.2:n.170-32C>T | |
NM_000432.4:c.170-32C>T MANE Select | NP_000423.2:n.170-32C>T |