HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110919117T= , CM000674.2:g.110919117T= | GRCh38 |
NC_000012.11:g.111356921T= , CM000674.1:g.111356921T= | GRCh37 |
NC_000012.10:g.109841304T= | NCBI36 |
NG_007554.1:g.6461A= , LRG_393:g.6461A= |
HGVS | Amino-acid Change |
---|---|
NM_000432.4:c.80A= MANE Select | NP_000423.2:p.Gln27= |
ENST00000228841.15:c.80A= MANE Select | ENSP00000228841.8:p.Gln27= |
NM_000432.3:c.80A= , LRG_393t1:c.80A= | NP_000423.2:p.Gln27= |
ENST00000228841.12:c.80A= | ENSP00000228841.7:p.Gln27= |
ENST00000546404.1:n.273A= | |
ENST00000548438.1:c.80A= | ENSP00000447154.1:p.Gln27= |
ENST00000663220.1:c.23A= | ENSP00000499568.1:p.Gln8= |