HGVS | Genome Assembly |
---|---|
NC_000002.12:g.188999358G= , CM000664.2:g.188999358G= | GRCh38 |
NC_000002.11:g.189864084G= , CM000664.1:g.189864084G= | GRCh37 |
NC_000002.10:g.189572329G= | NCBI36 |
NG_007404.1:g.29986G= , LRG_3:g.29986G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000450867.2:c.1997G= | ENSP00000415346.2:p.Gly666= | |
ENST00000304636.9:c.2096G= MANE Select | ENSP00000304408.4:p.Gly699= | |
ENST00000304636.7:c.2096G= | ENSP00000304408.3:p.Gly699= | |
ENST00000317840.9:c.2096G= | ENSP00000315243.6:p.Gly699= | |
NM_000090.3:c.2096G= , LRG_3t1:c.2096G= | NP_000081.1:p.Gly699= | |
NM_000090.4:c.2096G= MANE Select | NP_000081.2:p.Gly699= |