HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94067470G>T , CM000663.2:g.94067470G>T | GRCh38 |
NC_000001.10:g.94533026G>T , CM000663.1:g.94533026G>T | GRCh37 |
NC_000001.9:g.94305614G>T | NCBI36 |
NG_009073.1:g.58680C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.1555-4153C>A MANE Select | ENSP00000359245.3:n.1555-4153C>A | |
ENST00000649773.1:c.1555-4153C>A | ENSP00000496882.1:n.1555-4153C>A | |
ENST00000370225.3:c.1555-4153C>A | ENSP00000359245.3:n.1555-4153C>A | |
NM_000350.2:c.1555-4153C>A | NP_000341.2:n.1555-4153C>A | |
NM_000350.3:c.1555-4153C>A MANE Select | NP_000341.2:n.1555-4153C>A |