HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110911094C= , CM000674.2:g.110911094C= | GRCh38 |
NC_000012.11:g.111348898C= , CM000674.1:g.111348898C= | GRCh37 |
NC_000012.10:g.109833281C= | NCBI36 |
NG_007554.1:g.14484G= , LRG_393:g.14484G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000228841.15:c.484G= MANE Select | ENSP00000228841.8:p.Gly162= | |
ENST00000663220.1:c.427G= | ENSP00000499568.1:p.Gly143= | |
ENST00000228841.12:c.484G= | ENSP00000228841.7:p.Gly162= | |
ENST00000548438.1:c.442G= | ENSP00000447154.1:p.Gly148= | |
NM_000432.3:c.484G= , LRG_393t1:c.484G= | NP_000423.2:p.Gly162= | |
NM_000432.4:c.484G= MANE Select | NP_000423.2:p.Gly162= |